NDC 68382-132 – Tamsulosin Hydrochloride
Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral
Product NDC68382-132
Product details
- Brand name
- Tamsulosin Hydrochloride
- Generic name
- Tamsulosin Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078225
- Marketed since
- April 27, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker
Active ingredients
- Tamsulosin Hydrochloride .4 mg/1
Uses, dosage, side effects and warnings for Tamsulosin Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 68382-132-01 | 100 CAPSULE in 1 BOTTLE (68382-132-01) | Apr 27, 2010 |
| 68382-132-05 | 500 CAPSULE in 1 BOTTLE (68382-132-05) | Apr 27, 2010 |
| 68382-132-06 | 30 CAPSULE in 1 BOTTLE (68382-132-06) | Apr 27, 2010 |
| 68382-132-10 | 1000 CAPSULE in 1 BOTTLE (68382-132-10) | Apr 27, 2010 |
| 68382-132-14 | 60 CAPSULE in 1 BOTTLE (68382-132-14) | Apr 27, 2010 |
| 68382-132-16 | 90 CAPSULE in 1 BOTTLE (68382-132-16) | Apr 27, 2010 |
| 68382-132-77 | 100 BLISTER PACK in 1 CARTON (68382-132-77) / 1 CAPSULE in 1 BLISTER PACK (68382-132-30) | Apr 27, 2010 |
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