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
- 68788-8866_103080cb-6381-44f6-8a31-1fc81e7c890f
- Product NDC
- 68788-8866
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250423
- 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, EXTENDED RELEASE in 1 BOTTLE (68788-8866-1) · 68788-8866-1
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-3) · 68788-8866-3
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-6) · 68788-8866-6
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-8) · 68788-8866-8
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8866-9) · 68788-8866-9
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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