Prazosin Hydrochloride
- Product NDC
- 70518-0241
- 11-digit product format
- 705180241
- Labeler code
- 70518
- Product ID
- 70518-0241_e0dfa6ca-b314-25cb-e053-2a95a90a12cc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 2017-02-20
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 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 |
|---|
| 70518-0241-0 | 70518024100 | 30 CAPSULE in 1 BLISTER PACK (70518-0241-0) | 30 capsule | 2017-02-20 | 0000-00-00 | No | No | Current |