Tamsulosin Hydrochloride
- Product NDC
- 72162-2217
- 11-digit product format
- 721622217
- Labeler code
- 72162
- Product ID
- 72162-2217_e52bdf8c-81eb-4b77-a598-d8709e95b8a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tamsulosin Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TAMSULOSIN HYDROCHLORIDE | .4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 11SV1951MR |
| Rxcui | 863669 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2217-5 | Tamsulosin Hydrochloride | 500 in 1 BOTTLE | CAPSULE | 500 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2217 | TAMSULOSIN HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20240106_fd73ddfd-3773-45b2-9795-9e58744a6803.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2217-5 | 72162221705 | 500 CAPSULE in 1 BOTTLE (72162-2217-5) | 500 capsule | 2013-04-30 | No | No | Historical |