Tamsulosin hydrochloride
- Product NDC
- 73750-099
- 11-digit product format
- 737500099
- Labeler code
- 73750
- Product ID
- 73750-099_d9e79735-f262-407b-e053-2995a90a637d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- QYK BRANDS LLC
- Application
- ANDA211885
- Marketing category
- ANDA
- Marketing start
- 2022-02-02
- Marketing end
- 0000-00-00
- Substance
- TAMSULOSIN HYDROCHLORIDE
- Active strength
- 0 mg/.4mg
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 73750-099-10 | Tamsulosin hydrochloride | 100 mg in 1 BOTTLE | CAPSULE | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73750-099 | TAMSULOSIN HYDROCHLORIDE CAPSULE [QYK BRANDS LLC] | 6 | Legacy NDC, 1 package rows | 20230203_d6e4cf51-e8cb-08c4-e053-2a95a90aefd7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73750-099-01 | 73750009901 | 1000 mg in 1 BOTTLE (73750-099-01) | 1000 mg | 2022-02-28 | 0000-00-00 | No | No | Current |
| 73750-099-10 | 73750009910 | 100 mg in 1 BOTTLE (73750-099-10) | 100 mg | 2022-02-02 | 0000-00-00 | No | No | Current |
| 73750-099-90 | 73750009990 | 90 mg in 1 BOTTLE (73750-099-90) | 90 mg | 2022-02-28 | 0000-00-00 | No | No | Current |