NDC 67877-450 – Tamsulosin Hydrochloride
Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral
Product NDC67877-450
Product details
- Brand name
- Tamsulosin Hydrochloride
- Generic name
- Tamsulosin Hydrochloride
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA207405
- Marketed since
- August 11, 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 67877-450-01 | 100 CAPSULE in 1 BOTTLE (67877-450-01) | Aug 11, 2017 |
| 67877-450-05 | 500 CAPSULE in 1 BOTTLE (67877-450-05) | Aug 11, 2017 |
| 67877-450-10 | 1000 CAPSULE in 1 BOTTLE (67877-450-10) | Aug 11, 2017 |
| 67877-450-30 | 30 CAPSULE in 1 BOTTLE (67877-450-30) | Aug 11, 2017 |
| 67877-450-38 | 10 BLISTER PACK in 1 CARTON (67877-450-38) / 10 CAPSULE in 1 BLISTER PACK (67877-450-33) | Aug 11, 2017 |
| 67877-450-60 | 60 CAPSULE in 1 BOTTLE (67877-450-60) | Aug 11, 2017 |
Recalls mentioning this NDC
- D-1066-2019 Mar 13, 2019 · Class II
Failed Dissolution Specifications: High Out-of-Specification dissolution results were observed during stability testing.
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