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
- 68382-758_278de28c-b40d-4fb7-802e-24b98e9de3b2
- Product NDC
- 68382-758
- Form
- TABLET, FILM COATED
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141209
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68382-758-01) · 68382-758-01
- 500 TABLET, FILM COATED in 1 BOTTLE (68382-758-05) · 68382-758-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (68382-758-10) · 68382-758-10
- 90 TABLET, FILM COATED in 1 BOTTLE (68382-758-16) · 68382-758-16
- 100 BLISTER PACK in 1 CARTON (68382-758-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-758-30) · 68382-758-77
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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