NDC 59651-063 – Dutasteride and Tamsulosin Hydrochloride
Dutasteride .5 mg/1; Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral
Product NDC59651-063
Product details
- Brand name
- Dutasteride and Tamsulosin Hydrochloride
- Generic name
- Dutasteride and Tamsulosin Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA213300
- Marketed since
- July 18, 2024
- 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 |
|---|---|---|
| 59651-063-30 | 30 CAPSULE in 1 BOTTLE (59651-063-30) | Jul 18, 2024 |
| 59651-063-90 | 90 CAPSULE in 1 BOTTLE (59651-063-90) | Jul 18, 2024 |
Other Dutasteride and tamsulosin hydrochloride products
- 70771-1356 Dutasteride .5 mg/1; Tamsulosin Hydrochloride .4 mg/1 · Capsule · Zydus Lifesciences Limited
- 68382-640 Dutasteride .5 mg/1; Tamsulosin Hydrochloride .4 mg/1 · Capsule · Zydus Pharmaceuticals USA Inc.