NDC 71335-3020 – Pioglitazone and metformin hydrochloride
Pioglitazone Hydrochloride 15 mg/1; Metformin Hydrochloride 850 mg/1 · Tablet · Oral
Product NDC71335-3020
Product details
- Brand name
- Pioglitazone and metformin hydrochloride
- Generic name
- Pioglitazone and metformin hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA204802
- Marketed since
- November 6, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide; Peroxisome Proliferator Receptor alpha Agonist; Peroxisome Proliferator Receptor gamma Agonist; Thiazolidinedione
Active ingredients
- Pioglitazone Hydrochloride 15 mg/1
- Metformin Hydrochloride 850 mg/1
Uses, dosage, side effects and warnings for Pioglitazone and metformin hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3020-1 | 180 TABLET in 1 BOTTLE (71335-3020-1) | Dec 3, 2025 |
Other Pioglitazone and metformin hydrochloride products
- 71335-3019 Pioglitazone Hydrochloride 15 mg/1; Metformin Hydrochloride 500 mg/1 · Tablet · Bryant Ranch Prepack
- 33342-176 Metformin Hydrochloride 500 mg/1; Pioglitazone Hydrochloride 15 mg/1 · Tablet · Macleods Pharmaceuticals Limited
- 33342-177 Metformin Hydrochloride 850 mg/1; Pioglitazone Hydrochloride 15 mg/1 · Tablet · Macleods Pharmaceuticals Limited