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
- 71205-882_27a10d92-3e03-4881-9b8f-7d0ee57cb744
- Product NDC
- 71205-882
- Form
- TABLET, FILM COATED
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171121
- Source listing expiry
- 20261231
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, PLASTIC (71205-882-00) · 71205-882-00
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-11) · 71205-882-11
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-30) · 71205-882-30
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-55) · 71205-882-55
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-60) · 71205-882-60
- 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-64) · 71205-882-64
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-72) · 71205-882-72
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-78) · 71205-882-78
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-882-90) · 71205-882-90
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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