Tamsulosin Hydrochloride
- Product NDC
- 67046-720
- 11-digit product format
- 670460720
- Labeler code
- 67046
- Product ID
- 67046-720_7350ad6e-7745-4743-9aa4-2a14ff01fef4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA078225
- Marketing category
- ANDA
- Marketing start
- 2010-07-28
- 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 |
|---|
| 67046-720-30 | Tamsulosin Hydrochloride | 30 in 1 BLISTER PACK | CAPSULE | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-720 | TAMSULOSIN HYDROCHLORIDE CAPSULE [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20100728_7350ad6e-7745-4743-9aa4-2a14ff01fef4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-720-30 | 67046072030 | 30 in 1 BLISTER PACK | Historical |