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
- 70518-3084_5838e3ba-b64f-6ab5-e063-6294a90aa2e4
- Product NDC
- 70518-3084
- Form
- TABLET
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210504
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 850 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BLISTER PACK (70518-3084-3) · 70518-3084-3
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-3084-4) · 70518-3084-4
- 180 TABLET in 1 BOTTLE, PLASTIC (70518-3084-6) · 70518-3084-6
- 100 TABLET in 1 BOTTLE, PLASTIC (70518-3084-7) · 70518-3084-7
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 →