United States · FDA National Drug Code directory

DAPAGLIFLOZIN

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
62332-393_0596c9b4-b2c1-44d5-9f2a-7ea2c6cfb2ac
Product NDC
62332-393
Form
TABLET, FILM COATED
Composition / generic term
DAPAGLIFLOZIN
Labeler
Alembic Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260406
Source listing expiry
20271231

Source-listed ingredients

  • DAPAGLIFLOZIN — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (62332-393-30) · 62332-393-30
  • 90 TABLET, FILM COATED in 1 BOTTLE (62332-393-90) · 62332-393-90
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-393-91) · 62332-393-91

Source and coverage

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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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