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
- 62135-683_570c5a61-a145-01f8-e063-6394a90acba5
- Product NDC
- 62135-683
- Form
- TABLET
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- Chartwell RX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020124
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 850 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (62135-683-05) · 62135-683-05
- 1000 TABLET in 1 BOTTLE (62135-683-10) · 62135-683-10
- 180 TABLET in 1 BOTTLE (62135-683-18) · 62135-683-18
- 30 TABLET in 1 BOTTLE (62135-683-30) · 62135-683-30
- 90 TABLET in 1 BOTTLE (62135-683-90) · 62135-683-90
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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