NDC 71335-0886 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-0886
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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 (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0886-1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-1) | Aug 20, 2018 |
| 71335-0886-2 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-2) | Dec 27, 2021 |
| 71335-0886-3 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-3) | Jul 17, 2018 |
| 71335-0886-4 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-4) | Aug 7, 2018 |
| 71335-0886-5 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-5) | Jun 28, 2018 |
| 71335-0886-6 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-6) | Dec 27, 2021 |
| 71335-0886-7 | 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-7) | Dec 27, 2021 |
| 71335-0886-8 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-8) | Dec 27, 2021 |
| 71335-0886-9 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-9) | Dec 27, 2021 |
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