United States · FDA National Drug Code directory

AVGEMSI

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
83831-123_42b97c44-15f5-4d38-b382-bbc1b2e654d0
Product NDC
83831-123
Form
INJECTION, SOLUTION
Composition / generic term
Gemcitabine
Labeler
Avyxa Pharma, LLC
Marketing category
NDA
Marketing start / end (source format)
20250803
Source listing expiry
20271231

Source-listed ingredients

  • GEMCITABINE HYDROCHLORIDE — 38 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, MULTI-DOSE in 1 CARTON (83831-123-01) / 26.3 mL in 1 VIAL, MULTI-DOSE · 83831-123-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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