NDC 33342-159 – Tamsulosin Hydrochloride
Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral
Product NDC33342-159
Product details
- Brand name
- Tamsulosin Hydrochloride
- Generic name
- Tamsulosin Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA204645
- Marketed since
- January 25, 2017
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 33342-159-07 | 30 CAPSULE in 1 BOTTLE (33342-159-07) | Jan 25, 2017 |
| 33342-159-11 | 100 CAPSULE in 1 BOTTLE (33342-159-11) | Jan 25, 2017 |
| 33342-159-12 | 10 BLISTER PACK in 1 CARTON (33342-159-12) / 10 CAPSULE in 1 BLISTER PACK | Jan 25, 2017 |
| 33342-159-15 | 500 CAPSULE in 1 BOTTLE (33342-159-15) | Jan 25, 2017 |
| 33342-159-44 | 1000 CAPSULE in 1 BOTTLE (33342-159-44) | Jan 25, 2017 |
Recalls mentioning this NDC
- D-1844-2019 Aug 21, 2019 · Class II
Failed Dissolution Specifications
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