NDC 70771-1356 – Dutasteride and tamsulosin hydrochloride
Dutasteride .5 mg/1; Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral
Product NDC70771-1356
Product details
- Brand name
- Dutasteride and tamsulosin hydrochloride
- Generic name
- Dutasteride and tamsulosin hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA207769
- Marketed since
- June 4, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- 5-alpha Reductase Inhibitor; alpha-Adrenergic Blocker
Active ingredients
- Dutasteride .5 mg/1
- Tamsulosin Hydrochloride .4 mg/1
Uses, dosage, side effects and warnings for Dutasteride and tamsulosin hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1356-3 | 30 CAPSULE in 1 BOTTLE (70771-1356-3) | Jun 4, 2018 |
| 70771-1356-9 | 90 CAPSULE in 1 BOTTLE (70771-1356-9) | Jun 4, 2018 |