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
- 25000-134_6e1fd481-e776-4e5c-a9d3-736b6e4e88fe
- Product NDC
- 25000-134
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- MARKSANS PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120601
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (25000-134-03) · 25000-134-03
- 1000 TABLET, FILM COATED in 1 BOTTLE (25000-134-14) · 25000-134-14
- 2600 TABLET, FILM COATED in 1 BAG (25000-134-51) · 25000-134-51
- 1 BAG in 1 BOX (25000-134-98) / 16455 TABLET, FILM COATED in 1 BAG · 25000-134-98
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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