TAMSULOSIN HYDROCHLORIDE
- Product NDC
- 70934-969
- 11-digit product format
- 709340969
- Labeler code
- 70934
- Product ID
- 70934-969_df725436-bd23-a119-e053-2a95a90ac79e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TAMSULOSIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA078938
- Marketing category
- ANDA
- Marketing start
- 2022-05-19
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70934-969-30 | 70934096930 | 30 CAPSULE in 1 BOTTLE, PLASTIC (70934-969-30) | 30 capsule | 2022-05-19 | 0000-00-00 | No | No | Current |
| 70934-969-90 | 70934096990 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70934-969-90) | 90 capsule | 2022-05-19 | 0000-00-00 | No | No | Current |