NDC 71610-837 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral
Product NDC71610-837
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- metformin hydrochloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA201991
- Marketed since
- March 1, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71610-837-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-30) | May 31, 2024 |
| 71610-837-53 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-53) | May 31, 2024 |
| 71610-837-60 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-60) | May 31, 2024 |
| 71610-837-70 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-70) | May 31, 2024 |
| 71610-837-80 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-80) | May 31, 2024 |
| 71610-837-94 | 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-837-94) | May 31, 2024 |
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