Tamsulosin Hydrochloride
- Product NDC
- 70934-328
- 11-digit product format
- 709340328
- Labeler code
- 70934
- Product ID
- 70934-328_b7b1779e-3d36-c89b-e053-2a95a90a89e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA090931
- Marketing category
- ANDA
- Marketing start
- 2019-04-01
- 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
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-328-30 | 70934032830 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-328-30) | 30 capsule | 2019-08-20 | 0000-00-00 | No | No | Current |
| 70934-328-90 | 70934032890 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70934-328-90) | 90 capsule | 2019-04-01 | 0000-00-00 | No | No | Current |