NDC 70010-492 – Metformin
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC70010-492
Product details
- Brand name
- Metformin
- Generic name
- Metformin ER 750 mg
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209313
- Marketed since
- July 31, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 70010-492-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-492-01) | Jul 31, 2018 |
| 70010-492-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-492-05) | Jul 31, 2018 |
| 70010-492-20 | 3500 TABLET, EXTENDED RELEASE in 1 POUCH (70010-492-20) | Jun 14, 2019 |
| 70010-492-21 | 17500 TABLET, EXTENDED RELEASE in 1 CARTON (70010-492-21) | Jun 14, 2019 |
Recalls mentioning this NDC
- D-1386-2020 Jul 22, 2020 · Class II
CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level
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