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Therapeutic Area

Anticoagulant

Therapeutic area intelligence for Anticoagulant with 22 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
22
Catalysts
0
Companies
8

Companies

AstraZeneca →
Bristol Myers Squibb →
Eugia Pharma →
Hikma Pharma →
Mankind Pharma →
Micro Labs →
Sandoz →
Teva →

Assets

Apixaban →
Argatroban →
AZURITY →
Cipla →
Eliquis →
FDA →
Hospira →
Ondexxya →
Rivaroxaban →
Viatris →

Recent signals(22)

RegulatoryJuly 23, 2026

FDA Accepts Supplemental Application for Argatroban by Fresenius Kabi

The FDA has accepted a supplemental application for Argatroban submitted by Fresenius Kabi.

RegulatoryJuly 22, 2026

FDA Accepts Supplemental NDA for Argatroban in Dextrose by Sandoz

The FDA has accepted a supplemental NDA for Argatroban in Dextrose submitted by Sandoz.

RegulatoryJuly 20, 2026

FDA Accepts Supplemental NDA for Argatroban by Accord Healthcare

The FDA has accepted a supplemental NDA for Argatroban in Sodium Chloride submitted by Accord Healthcare.

RegulatoryJuly 20, 2026

FDA mandates compliance for imported Heparin Sodium with USP specifications

The FDA is enforcing compliance for all imported Heparin Sodium to meet the latest USP specifications.

RegulatoryJuly 19, 2026

FDA Accepts Supplemental NDA for Argatroban by Hikma Pharma

The FDA has accepted a supplemental NDA for Argatroban submitted by Hikma Pharma.

RegulatoryJuly 18, 2026

Hospira's Heparin Sodium ANDA090571 Receives AP Status from FDA

The FDA has granted an Abbreviated New Drug Application (ANDA) approval status for Heparin Sodium submitted by Hospira Inc.

RegulatoryJuly 18, 2026

FDA Grants AP Status for Heparin Sodium ANDA088100 from Hospira

The FDA has granted Abbreviated Approval (AP) status for Heparin Sodium under ANDA088100 submitted by Hospira.

StrategyJuly 18, 2026

FDA Grants AP Status for Hospira's Heparin Sodium Preservative Free

The FDA has granted an Abbreviated New Drug Application (ANDA) approval status for Hospira's Heparin Sodium Preservative Free.

ClinicalJuly 17, 2026

Study on Rivaroxaban's Effects in Peripheral Artery Disease Initiated

A clinical trial is underway to assess the impact of rivaroxaban on symptoms of peripheral artery disease.

RegulatoryJuly 16, 2026

FDA Approves Supplemental NDA for Argatroban by Fresenius Kabi

The FDA has approved a supplemental NDA for Argatroban submitted by Fresenius Kabi.

RegulatoryJuly 10, 2026

FDA Approval Application for Rivaroxaban by Mankind Pharma

Mankind Pharma has submitted an application for Rivaroxaban under ANDA220874, currently under standard review.

StrategyJuly 9, 2026

FDA Grants Approval for Rivaroxaban Generic by Micro Labs

The FDA has granted approval for the generic version of Rivaroxaban submitted by Micro Labs.

ClinicalJuly 8, 2026

AstraZeneca Investigates Safety of Ondexxya IV Injection in Real-World Use

AstraZeneca is conducting a survey to assess the safety and effectiveness of Ondexxya IV Injection 200 mg in real-world conditions.

RegulatoryJuly 8, 2026

FDA Submission Status Update for ABANTA (Apixaban) by AZURITY

The FDA has received a submission for ABANTA (Apixaban) under NDA221024 from AZURITY, currently under standard review.

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 Accepts Supplemental Application for Eliquis (Apixaban)

The FDA has accepted a supplemental application for Eliquis, indicating ongoing development and potential label updates.

RegulatoryJune 28, 2026

Sandoz Issues Class 4 Medicines Defect Notification for Apixaban Tablets

Sandoz Ltd. reported that the Patient Information Leaflet for certain batches of Apixaban tablets lacks up-to-date information.

RegulatoryJune 23, 2026

Viatris Reports Quality Defect in Arixtra Pre-Filled Syringes

Viatris has identified a quality defect in Arixtra pre-filled syringes, with reports of brown discolouration and blockage due to needle oxidation.

RegulatoryJune 23, 2026

FDA Accepts Supplemental Application for Argatroban by Sandoz

The FDA has accepted a supplemental application for Argatroban submitted by Sandoz.

RegulatoryJune 21, 2026

Cipla's NDA for Argatroban in Sodium Chloride Receives AP Status from FDA

Cipla's supplemental NDA for Argatroban in Sodium Chloride has been granted an Approval Pending (AP) status by the FDA.

RegulatoryJune 21, 2026

FDA Accepts Supplemental NDA for Argatroban in Sodium Chloride

The FDA has accepted a supplemental NDA for Argatroban in Sodium Chloride submitted by Eugia Pharma.

Upcoming catalysts

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Indications

No related entities indexed yet.

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