NDC 72578-036 – Metformin Hydrochloride
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC72578-036
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Viona Pharmaceuticals Inc
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077078
- Marketed since
- March 15, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 72578-036-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-01) | Mar 15, 2019 |
| 72578-036-05 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72578-036-05) | Mar 15, 2019 |
Recalls mentioning this NDC
- D-0392-2022 Feb 2, 2022 · Class II
CGMP Deviations- Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit. - D-0640-2021 Jun 30, 2021 · Class II
CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.
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