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
- 62135-680_570c5a61-a145-01f8-e063-6394a90acba5
- Product NDC
- 62135-680
- 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 — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET in 1 BOTTLE (62135-680-05) · 62135-680-05
- 1000 TABLET in 1 BOTTLE (62135-680-10) · 62135-680-10
- 180 TABLET in 1 BOTTLE (62135-680-18) · 62135-680-18
- 60 TABLET in 1 BOTTLE (62135-680-60) · 62135-680-60
- 90 TABLET in 1 BOTTLE (62135-680-90) · 62135-680-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →