Prazosin Hydrochloride
- Product NDC
- 70518-1756
- 11-digit product format
- 705181756
- Labeler code
- 70518
- Product ID
- 70518-1756_d331e9eb-c47e-6057-e053-2a95a90a9aaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- alpha-Adrenergic Blocker [EPC],Adrenergic alpha-Antagonists [MoA]
- 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 |
|---|
| 70518-1756-1 | 70518175601 | 60 CAPSULE in 1 BLISTER PACK (70518-1756-1) | 60 capsule | 2021-12-14 | 0000-00-00 | No | No | Current |