tamsulosin hydrochloride
- Product NDC
- 70518-1999
- 11-digit product format
- 705181999
- Labeler code
- 70518
- Product ID
- 70518-1999_c5984fa3-c4aa-0629-e053-2a95a90a5173
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tamsulosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078015
- Marketing category
- ANDA
- Marketing start
- 2019-04-02
- 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
- 2022-12-31
- 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 |
|---|
| 70518-1999-0 | 70518199900 | 28 CAPSULE in 1 BLISTER PACK (70518-1999-0) | 28 capsule | 2019-04-02 | 0000-00-00 | No | No | Current |
| 70518-1999-1 | 70518199901 | 30 CAPSULE in 1 BLISTER PACK (70518-1999-1) | 30 capsule | 2020-05-04 | 0000-00-00 | No | No | Current |