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
- 63187-779_103cbde3-9398-44e5-b27e-c4c77a46e97a
- Product NDC
- 63187-779
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metformin hydrochloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130301
- 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, EXTENDED RELEASE in 1 BOTTLE (63187-779-30) · 63187-779-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-779-60) · 63187-779-60
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-779-78) · 63187-779-78
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-779-90) · 63187-779-90
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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