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
- 43353-982_4900492c-70fa-e5b5-e063-6294a90af743
- Product NDC
- 43353-982
- Form
- TABLET
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130911
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (43353-982-30) · 43353-982-30
- 60 TABLET in 1 BOTTLE (43353-982-53) · 43353-982-53
- 90 TABLET in 1 BOTTLE (43353-982-60) · 43353-982-60
- 120 TABLET in 1 BOTTLE (43353-982-70) · 43353-982-70
- 180 TABLET in 1 BOTTLE (43353-982-80) · 43353-982-80
- 270 TABLET in 1 BOTTLE (43353-982-92) · 43353-982-92
- 360 TABLET in 1 BOTTLE (43353-982-94) · 43353-982-94
- 450 TABLET in 1 BOTTLE (43353-982-96) · 43353-982-96
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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