Tamsulosin Hydrochloride
- Product NDC
- 68071-5118
- 11-digit product format
- 680715118
- Labeler code
- 68071
- Product ID
- 68071-5118_1b46ae21-226e-0f42-e063-6294a90a685e
- 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
- Substance
- TAMSULOSIN HYDROCHLORIDE
- Active strength
- .4 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 68071-5118-1 | 68071511801 | 100 CAPSULE in 1 BOTTLE (68071-5118-1) | 100 capsule | 2019-11-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tamsulosin Hydrochloride | NuCare Pharmaceuticals,Inc. | 2024-06-19 | HUMAN PRESCRIPTION DRUG LABEL | 3 |