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
- 72189-219_4c4c00bb-696d-96d9-e063-6394a90aba0e
- Product NDC
- 72189-219
- Form
- TABLET
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- direct rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210526
- 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 in 1 BOTTLE (72189-219-30) · 72189-219-30
- 60 TABLET in 1 BOTTLE (72189-219-60) · 72189-219-60
- 180 TABLET in 1 BOTTLE (72189-219-82) · 72189-219-82
- 90 TABLET in 1 BOTTLE (72189-219-90) · 72189-219-90
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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