Tamsulosin Hydrochloride
- Product NDC
- 70518-2541
- 11-digit product format
- 705182541
- Labeler code
- 70518
- Product ID
- 70518-2541_dd8ded90-ac3e-ac8c-e053-2a95a90a9c59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA204645
- Marketing category
- ANDA
- Marketing start
- 2020-01-13
- 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2541-0 | 70518254100 | 30 CAPSULE in 1 BLISTER PACK (70518-2541-0) | 30 capsule | 2020-01-13 | 0000-00-00 | No | No | Current |
| 70518-2541-1 | 70518254101 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2541-1) | 90 capsule | 2020-04-28 | 0000-00-00 | No | No | Current |
| 70518-2541-2 | 70518254102 | 30 CAPSULE in 1 BLISTER PACK (70518-2541-2) | 30 capsule | 2022-03-15 | 0000-00-00 | No | No | Current |
| 70518-2541-3 | 70518254103 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2541-3) | 90 capsule | 2022-04-22 | 0000-00-00 | No | No | Current |