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Therapeutic Area

Sedative

Therapeutic area intelligence for Sedative with 9 indexed intelligence signals across regulatory, clinical, competitive, and market developments.

Signals
9
Catalysts
0
Companies
2

Companies

Hikma →
HQ SPCLT Pharma →

Assets

Baxter →
dexmedetomidine →
FDA →
Hospira →
Zydus →

Recent signals(9)

RegulatoryAugust 14, 2026

Hikma's Sodium Butabarbital ANDA085432 Receives AP Status from FDA

Hikma's Abbreviated New Drug Application (ANDA085432) for Sodium Butabarbital has received an Approved Product (AP) status from the FDA.

Regulatory
August 14, 2026

Hikma's Sodium Butabarbital ANDA085418 Receives AP Status from FDA

Hikma's ANDA085418 for Sodium Butabarbital has received Abbreviated Approval (AP) status from the FDA.

RegulatoryAugust 3, 2026

FDA Accepts Supplement for Dexmedetomidine Hydrochloride NDA 206628

The FDA has accepted a supplemental application for Dexmedetomidine Hydrochloride under NDA 206628.

RegulatoryAugust 2, 2026

FDA grants supplemental approval for PRECEDEX (dexmedetomidine hydrochloride)

The FDA has granted supplemental approval for PRECEDEX, a sedative agent, under NDA021038.

RegulatoryJuly 27, 2026

FDA Grants Approval for Dexmedetomidine Hydrochloride by Baxter Healthcare

The FDA has granted approval for Dexmedetomidine Hydrochloride under application ANDA208103 submitted by Baxter Healthcare.

RegulatoryJuly 23, 2026

Zydus Pharms receives AP status for Dexmedetomidine Hydrochloride ANDA206798

Zydus Pharms has received an Abbreviated New Drug Application (ANDA) approval status for Dexmedetomidine Hydrochloride.

RegulatoryJuly 12, 2026

FDA Accepts Supplemental NDA for Dexmedetomidine Hydrochloride

The FDA has accepted a supplemental NDA for Dexmedetomidine Hydrochloride submitted by HQ SPCLT PHARMA.

RegulatoryJuly 12, 2026

FDA Accepts Supplement for PRECEDEX (Dexmedetomidine Hydrochloride)

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

RegulatoryJuly 4, 2026

Baxter Healthcare's Dexmedetomidine Hydrochloride ANDA208103 Receives AP Status

Baxter Healthcare Corporation's application for Dexmedetomidine Hydrochloride has received an Abbreviated Approval (AP) status from the FDA.

Upcoming catalysts

No catalysts indexed for this entity yet.

Indications

No related entities indexed yet.

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