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
- 43063-544_413942f3-9d8b-ea87-e063-6394a90aeb7f
- Product NDC
- 43063-544
- Form
- TABLET
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121217
- Source listing expiry
- 20261231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-544-30) · 43063-544-30
- 60 TABLET in 1 BOTTLE, PLASTIC (43063-544-60) · 43063-544-60
- 90 TABLET in 1 BOTTLE, PLASTIC (43063-544-90) · 43063-544-90
- 180 TABLET in 1 BOTTLE, PLASTIC (43063-544-93) · 43063-544-93
- 120 TABLET in 1 BOTTLE, PLASTIC (43063-544-98) · 43063-544-98
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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