Tamsulosin Hydrochloride
- Product NDC
- 68071-2508
- 11-digit product format
- 680712508
- Labeler code
- 68071
- Product ID
- 68071-2508_ca0084a2-5c99-0ce3-e053-2a95a90abe64
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA202433
- Marketing category
- ANDA
- Marketing start
- 2013-04-30
- Marketing end
- 0000-00-00
- Substance
- TAMSULOSIN HYDROCHLORIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 11SV1951MR | TAMSULOSIN HYDROCHLORIDE | 106463-17-6 | TAMSULOSIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2508-1 | 68071250801 | 100 CAPSULE in 1 BOTTLE (68071-2508-1) | 100 capsule | 2021-08-20 | 0000-00-00 | No | No | Current |