Tamsulosin Hydrochloride
- Product NDC
- 71205-688
- 11-digit product format
- 712050688
- Labeler code
- 71205
- Product ID
- 71205-688_58cba3d8-bb57-4e64-a191-dc050904c896
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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 |
|---|
| 71205-688-07 | 71205068807 | 7 CAPSULE in 1 BOTTLE (71205-688-07) | 7 capsule | 2022-08-22 | No | No | Historical |
| 71205-688-14 | 71205068814 | 14 CAPSULE in 1 BOTTLE (71205-688-14) | 14 capsule | 2022-08-22 | No | No | Historical |
| 71205-688-30 | 71205068830 | 30 CAPSULE in 1 BOTTLE (71205-688-30) | 30 capsule | 2022-08-22 | No | No | Historical |
| 71205-688-60 | 71205068860 | 60 CAPSULE in 1 BOTTLE (71205-688-60) | 60 capsule | 2022-08-22 | No | No | Historical |
| 71205-688-90 | 71205068890 | 90 CAPSULE in 1 BOTTLE (71205-688-90) | 90 capsule | 2022-08-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tamsulosin Hydrochloride | Proficient Rx LP | 2022-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |