Tamsulosin Hydrochloride
- Product NDC
- 70518-1417
- 11-digit product format
- 705181417
- Labeler code
- 70518
- Product ID
- 70518-1417_e67052a9-8134-1f3c-e053-2995a90a4a67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tamsulosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090931
- Marketing category
- ANDA
- Marketing start
- 2018-09-17
- 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 |
|---|
| 70518-1417-0 | 70518141700 | 28 CAPSULE in 1 BLISTER PACK (70518-1417-0) | 28 capsule | 2018-09-17 | 0000-00-00 | No | No | Current |
| 70518-1417-1 | 70518141701 | 30 CAPSULE in 1 BLISTER PACK (70518-1417-1) | 30 capsule | 2022-03-08 | 0000-00-00 | No | No | Current |