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: 65162-179_984302ad-793e-4f35-92da-e5e7f92154f6
Product NDC: 65162-179
Form: TABLET, EXTENDED RELEASE
Composition / generic term: Metformin Hydrochloride
Labeler: Amneal Pharmaceuticals LLC
Marketing category: ANDA
Marketing start / end (source format): 20100226
Source listing expiry: 20261231

Source-listed ingredients

METFORMIN HYDROCHLORIDE — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-03) · 65162-179-03
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-09) · 65162-179-09
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-10) · 65162-179-10
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-50) · 65162-179-50

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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