NDC 43063-902 – Metformin Hydrochloride Extended Release
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC43063-902
Product details
- Brand name
- Metformin Hydrochloride Extended Release
- Generic name
- Metformin Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090295
- Marketed since
- May 12, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Uses, dosage, side effects and warnings for Metformin Hydrochloride Extended Release →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 43063-902-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-902-30) | Mar 26, 2019 |
| 43063-902-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-902-60) | Nov 1, 2018 |
Recalls mentioning this NDC
- D-0060-2021 Nov 11, 2020 · Class II
CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level (per manufacturer)
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