Tamsulosin Hydrochloride
- Product NDC
- 66336-902
- 11-digit product format
- 663360902
- Labeler code
- 66336
- Product ID
- 66336-902_6b11fa9e-c8a5-4497-b5c5-13945879cdbb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Dispensing Solutions, Inc.
- Application
- ANDA090931
- Marketing category
- ANDA
- Marketing start
- 2010-07-15
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66336-902-07 | Tamsulosin Hydrochloride | 7 in 1 BOTTLE | CAPSULE | 7 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| TAMSULOSIN HYDROCHLORIDE | ACTIVE INGREDIENT | 11SV1951MR | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| TAMSULOSIN | ACTIVE MOIETY | G3P28OML5I | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| FERRIC OXIDE RED | INACTIVE INGREDIENT | 1K09F3G675 | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| GELATIN | INACTIVE INGREDIENT | 2G86QN327L | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S) | INACTIVE INGREDIENT | 24P2YXD2PW | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A | INACTIVE INGREDIENT | NX76LV5T8J | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
| TRIETHYL CITRATE | INACTIVE INGREDIENT | 8Z96QXD6UM | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-902 | TAMSULOSIN HYDROCHLORIDE CAPSULE [DISPENSING SOLUTIONS, INC.] | 1 | Legacy NDC, 1 package rows | 20130619_1d845218-1562-42a2-98fe-3b13cd5d0542.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-902-07 | 66336090207 | 7 in 1 BOTTLE | Historical |