United States · FDA National Drug Code directory

Metformin Hydrochloride

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
0904-7162_0bd2df04-cc80-405a-a0a9-05a627225d73
Product NDC
0904-7162
Form
TABLET
Composition / generic term
Metformin Hydrochloride
Labeler
Major Pharmaceuticals
Marketing category
ANDA
Marketing start / end (source format)
20190626
Source listing expiry
20271231

Source-listed ingredients

  • METFORMIN HYDROCHLORIDE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 CARTON (0904-7162-61) / 1 TABLET in 1 BLISTER PACK · 0904-7162-61

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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