NDC 68180-337 – Metformin Hydrochloride
Metformin Hydrochloride 1000 mg/1 · Tablet, Extended Release · Oral
Product NDC68180-337
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090692
- Marketed since
- September 30, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 1000 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68180-337-07 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-337-07) | Sep 30, 2011 |
Recalls mentioning this NDC
- D-1385-2020 Jul 22, 2020 · Class II
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
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