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Company

Teva

Pharmaceutical intelligence for Teva with 54 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
34
Catalysts
20
Assets
21

Recent signals(34)

RegulatoryAugust 6, 2026

Teva's Losartan Potassium Supplement Application Receives Standard Review Status

Teva's ANDA for Losartan Potassium has been submitted and is currently under standard review by the FDA.

StrategyAugust 5, 2026

Teva's Gabapentin ANDA075435 Receives AP Status from FDA

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Gabapentin.

StrategyAugust 3, 2026

Teva's Gabapentin ANDA205807 Receives AP Status from FDA

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval for Gabapentin.

Upcoming catalysts

No catalysts indexed for this entity yet.

Regulatory activity(22)

RegulatoryAugust 6, 2026

Teva's Losartan Potassium Supplement Application Receives Standard Review Status

Teva's ANDA for Losartan Potassium has been submitted and is currently under standard review by the FDA.

RegulatoryAugust 1, 2026

Teva's Sugammadex Sodium Receives FDA Approval Status

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Sugammadex Sodium.

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for Pomalidomide by Teva Pharmaceuticals

Teva Pharmaceuticals has submitted a supplemental application for Pomalidomide, which is currently under review by the FDA.

Clinical activity(3)

ClinicalJuly 6, 2026

Teva initiates trial for TEV-56286 assessing pharmacokinetics and safety

Teva is conducting a trial to evaluate the pharmacokinetics, safety, and tolerability of TEV-56286 in healthy participants.

ClinicalJune 21, 2026

Teva's TEV-56286 Trial for Multiple System Atrophy Underway

Teva is conducting a trial to evaluate the efficacy and safety of TEV-56286 in adults with Multiple System Atrophy.

ClinicalJune 19, 2026

Teva's TEV-53408 Trial for Vitiligo Focuses on Safety and Efficacy

Teva is conducting a trial to assess the safety and efficacy of TEV-53408 in adults with vitiligo over an 84-week period.

Competitive activity

No signals indexed for this entity yet.

Assets

AJOVY →
Argatroban →
Canagliflozin →
Copaxone →
Eltrombopag Olamine →
FDA →
Finasteride →
Gabapentin →
Junel FE →
Linagliptin →
Macitentan →
Morphine Sulfate →
Nilotinib Hydrochloride →
Pomalidomide →
Regulatory Approval →

Therapeutic areas

5-alpha reductase inhibitor →
Anesthesia →
Anticoagulant →
Anticonvulsant →
Antihypertensive →
Asthma →
Bisphosphonate →
Cardiology →
Cardiology · Pulmonary Arterial Hypertension →
Cardiovascular →
Cardiovascular · Anticoagulant →
Contraceptive →
COPD →

Indications

Asthma →
COPD →
Diabetes →
Metabolic Disorders →
Urea Cycle Disorder →
Urea Cycle Disorders →

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Regulatory
August 1, 2026

Teva's Sugammadex Sodium Receives FDA Approval Status

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Sugammadex Sodium.

RegulatoryJuly 30, 2026

FDA Accepts Supplemental Application for Pomalidomide by Teva Pharmaceuticals

Teva Pharmaceuticals has submitted a supplemental application for Pomalidomide, which is currently under review by the FDA.

RegulatoryJuly 30, 2026

FDA Acceptance of Supplemental NDA for ZIAC by Teva

The FDA has accepted a supplemental NDA for ZIAC, which contains bisoprolol fumarate and hydrochlorothiazide.

RegulatoryJuly 29, 2026

FDA Approves Supplemental NDA for ZIAC by Teva

The FDA has approved a supplemental NDA for ZIAC, which contains bisoprolol fumarate and hydrochlorothiazide.

StrategyJuly 29, 2026

FDA Submission Update for Canagliflozin by Teva Pharmaceuticals

Teva Pharmaceuticals has submitted an application for Canagliflozin under ANDA210451, currently under standard review.

RegulatoryJuly 29, 2026

FDA Accepts Application for Budesonide and Formoterol Fumarate Dihydrate

The FDA has accepted the application ANDA212212 for Budesonide and Formoterol Fumarate Dihydrate submitted by Teva Pharmaceuticals.

RegulatoryJuly 26, 2026

FDA Grants Approval for Glycerol Phenylbutyrate by Teva Pharmaceuticals

Teva Pharmaceuticals has received FDA approval for Glycerol Phenylbutyrate under application ANDA218738.

StrategyJuly 25, 2026

FDA Grants Approval for Teva's Tolvaptan ANDA216933

Teva Pharmaceuticals has received an approval for their Abbreviated New Drug Application (ANDA216933) for Tolvaptan.

StrategyJuly 24, 2026

Teva's ANDA Submission for Canagliflozin Receives TA Status

Teva Pharmaceuticals has submitted an ANDA for Canagliflozin, currently under standard review with TA status.

StrategyJuly 20, 2026

FDA Approval Application for Linagliptin by Teva Pharmaceuticals

Teva Pharmaceuticals has submitted an original application for Linagliptin under ANDA208433 with a standard review priority.

RegulatoryJuly 18, 2026

Teva's Eltrombopag Olamine ANDA209938 Receives Approval

Teva Pharmaceuticals has received approval for their ANDA209938 application for Eltrombopag Olamine.

RegulatoryJuly 13, 2026

Teva Pharmaceuticals Receives AP Status for Gabapentin Supplement

Teva Pharmaceuticals has received an Abbreviated Approval (AP) for a supplemental application for Gabapentin.

RegulatoryJuly 12, 2026

Teva's Gabapentin ANDA205807 Receives Approval Status from FDA

Teva Pharmaceuticals USA has received an approval status (AP) for its Abbreviated New Drug Application (ANDA205807) for Gabapentin.

StrategyJuly 9, 2026

Teva's Finasteride ANDA076511 Receives Abbreviated Approval from FDA

Teva's ANDA076511 for Finasteride has received an Abbreviated Approval from the FDA.

RegulatoryJuly 8, 2026

Teva's Nilotinib Hydrochloride ANDA219134 Receives AP Status from FDA

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Nilotinib Hydrochloride.

RegulatoryJuly 8, 2026

FDA Accepts Supplemental Application for Copaxone (Glatiramer Acetate)

The FDA has accepted a supplemental application for Copaxone, a treatment for multiple sclerosis.

RegulatoryJuly 7, 2026

Teva Pharmaceuticals submits supplemental application for Pomalidomide

Teva Pharmaceuticals has submitted a supplemental application for Pomalidomide under ANDA209956.

ClinicalJuly 6, 2026

Teva initiates trial for TEV-56286 assessing pharmacokinetics and safety

Teva is conducting a trial to evaluate the pharmacokinetics, safety, and tolerability of TEV-56286 in healthy participants.

StrategyJuly 5, 2026

Teva's Budesonide and Formoterol Fumarate Dihydrate Receives FDA Approval

Teva Pharmaceuticals has received FDA approval for ANDA212212, a generic formulation of Budesonide and Formoterol Fumarate Dihydrate.

RegulatoryJuly 3, 2026

Teva's Glycerol Phenylbutyrate ANDA218738 Receives AP Status from FDA

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Glycerol Phenylbutyrate.

RegulatoryJuly 3, 2026

FDA Accepts Supplemental Application for Argatroban by Teva Pharmaceuticals

The FDA has accepted a supplemental application for Argatroban in 0.9% sodium chloride submitted by Teva Pharmaceuticals.

RegulatoryJuly 1, 2026

Teva's Argatroban Supplement Receives FDA Acceptance

The FDA has accepted a supplemental application for Argatroban by Teva Pharmaceuticals.

RegulatoryJune 30, 2026

FDA Approves Supplemental Application for AJOVY (Fremanezumab)

The FDA has approved a supplemental application for AJOVY, a migraine treatment by Teva Pharmaceuticals.

RegulatoryJune 28, 2026

FDA Accepts Supplement Application for Teva's Morphine Sulfate

The FDA has accepted a supplemental application for Teva's Morphine Sulfate.

RegulatoryJune 27, 2026

Teva's ANDA219324 for Junel FE Receives Approval Status from FDA

Teva Pharmaceuticals' ANDA219324 for Junel FE has received an Approval Pending (AP) status from the FDA.

RegulatoryJune 27, 2026

FDA Approves Supplemental Application for Copaxone (Glatiramer Acetate)

The FDA has approved a supplemental application for Copaxone, a treatment for multiple sclerosis.

RegulatoryJune 25, 2026

FDA Approval Update for Teva's Tramadol Hydrochloride Supplement

Teva's supplemental application for Tramadol Hydrochloride has received an approval status from the FDA.

RegulatoryJune 23, 2026

FDA Grants AP Status for Teva's Risedronate Sodium Supplement

Teva Pharmaceuticals has received an Abbreviated Approval (AP) for a supplement of Risedronate Sodium.

StrategyJune 23, 2026

FDA Grants Approval for Macitentan ANDA211187 by Teva Pharmaceuticals

Teva Pharmaceuticals has received approval for its Abbreviated New Drug Application (ANDA211187) for Macitentan.

ClinicalJune 21, 2026

Teva's TEV-56286 Trial for Multiple System Atrophy Underway

Teva is conducting a trial to evaluate the efficacy and safety of TEV-56286 in adults with Multiple System Atrophy.

ClinicalJune 19, 2026

Teva's TEV-53408 Trial for Vitiligo Focuses on Safety and Efficacy

Teva is conducting a trial to assess the safety and efficacy of TEV-53408 in adults with vitiligo over an 84-week period.

RegulatoryJuly 30, 2026

FDA Acceptance of Supplemental NDA for ZIAC by Teva

The FDA has accepted a supplemental NDA for ZIAC, which contains bisoprolol fumarate and hydrochlorothiazide.

RegulatoryJuly 29, 2026

FDA Approves Supplemental NDA for ZIAC by Teva

The FDA has approved a supplemental NDA for ZIAC, which contains bisoprolol fumarate and hydrochlorothiazide.

RegulatoryJuly 29, 2026

FDA Accepts Application for Budesonide and Formoterol Fumarate Dihydrate

The FDA has accepted the application ANDA212212 for Budesonide and Formoterol Fumarate Dihydrate submitted by Teva Pharmaceuticals.

RegulatoryJuly 26, 2026

FDA Grants Approval for Glycerol Phenylbutyrate by Teva Pharmaceuticals

Teva Pharmaceuticals has received FDA approval for Glycerol Phenylbutyrate under application ANDA218738.

RegulatoryJuly 18, 2026

Teva's Eltrombopag Olamine ANDA209938 Receives Approval

Teva Pharmaceuticals has received approval for their ANDA209938 application for Eltrombopag Olamine.

RegulatoryJuly 13, 2026

Teva Pharmaceuticals Receives AP Status for Gabapentin Supplement

Teva Pharmaceuticals has received an Abbreviated Approval (AP) for a supplemental application for Gabapentin.

RegulatoryJuly 12, 2026

Teva's Gabapentin ANDA205807 Receives Approval Status from FDA

Teva Pharmaceuticals USA has received an approval status (AP) for its Abbreviated New Drug Application (ANDA205807) for Gabapentin.

RegulatoryJuly 8, 2026

Teva's Nilotinib Hydrochloride ANDA219134 Receives AP Status from FDA

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Nilotinib Hydrochloride.

RegulatoryJuly 8, 2026

FDA Accepts Supplemental Application for Copaxone (Glatiramer Acetate)

The FDA has accepted a supplemental application for Copaxone, a treatment for multiple sclerosis.

RegulatoryJuly 7, 2026

Teva Pharmaceuticals submits supplemental application for Pomalidomide

Teva Pharmaceuticals has submitted a supplemental application for Pomalidomide under ANDA209956.

RegulatoryJuly 3, 2026

Teva's Glycerol Phenylbutyrate ANDA218738 Receives AP Status from FDA

Teva Pharmaceuticals has received an Abbreviated New Drug Application (ANDA) approval status for Glycerol Phenylbutyrate.

RegulatoryJuly 3, 2026

FDA Accepts Supplemental Application for Argatroban by Teva Pharmaceuticals

The FDA has accepted a supplemental application for Argatroban in 0.9% sodium chloride submitted by Teva Pharmaceuticals.

RegulatoryJuly 1, 2026

Teva's Argatroban Supplement Receives FDA Acceptance

The FDA has accepted a supplemental application for Argatroban by Teva Pharmaceuticals.

RegulatoryJune 30, 2026

FDA Approves Supplemental Application for AJOVY (Fremanezumab)

The FDA has approved a supplemental application for AJOVY, a migraine treatment by Teva Pharmaceuticals.

RegulatoryJune 28, 2026

FDA Accepts Supplement Application for Teva's Morphine Sulfate

The FDA has accepted a supplemental application for Teva's Morphine Sulfate.

RegulatoryJune 27, 2026

Teva's ANDA219324 for Junel FE Receives Approval Status from FDA

Teva Pharmaceuticals' ANDA219324 for Junel FE has received an Approval Pending (AP) status from the FDA.

RegulatoryJune 27, 2026

FDA Approves Supplemental Application for Copaxone (Glatiramer Acetate)

The FDA has approved a supplemental application for Copaxone, a treatment for multiple sclerosis.

RegulatoryJune 25, 2026

FDA Approval Update for Teva's Tramadol Hydrochloride Supplement

Teva's supplemental application for Tramadol Hydrochloride has received an approval status from the FDA.

RegulatoryJune 23, 2026

FDA Grants AP Status for Teva's Risedronate Sodium Supplement

Teva Pharmaceuticals has received an Abbreviated Approval (AP) for a supplement of Risedronate Sodium.

Risedronate Sodium →
Symbicort →
TEV-53408 →
TEV-56286 →
Tolvaptan →
Tramadol Hydrochloride →
Dermatology →
Diabetes →
Diabetes · DPP-4 Inhibitor →
DPP-4 Inhibitor →
Hematology →
Hematology · Thrombocytopenia →
Hypertension →
Immunomodulator →
Metabolic Disorders →
Metabolic Disorders · Urea Cycle Disorder →
Migraine →
Multiple Sclerosis →
Multiple System Atrophy →
Nephrology →
Neurology →
Neurology · Anticonvulsant →
Neurology · Migraine →
Neurology · Multiple Sclerosis →
Neuromuscular Blockade →
Not specified →
Oncology →
Oncology · Immunomodulator →
Oncology · Tyrosine Kinase Inhibitor →
Opioid →
Osteoporosis →
Osteoporosis · Bisphosphonate →
Pain Management →
Pain Management · Opioid →
Pulmonary Arterial Hypertension →
Respiratory →
Respiratory · Asthma/COPD →
SGLT2 Inhibitor →
Small Molecule →
Thrombocytopenia →
Tyrosine Kinase Inhibitor →
Urea Cycle Disorder →
Urea Cycle Disorders →
Urology →
Urology · 5-alpha reductase inhibitor →
Vasopressin Antagonist →
Vitiligo →
Women's Health →
Women's Health · Contraceptive →