Prazosin Hydrochloride
- Product NDC
- 70518-3352
- 11-digit product format
- 705183352
- Labeler code
- 70518
- Product ID
- 70518-3352_d8110385-c7d7-5d97-e053-2995a90a5d3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2022-01-31
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 70518-3352-0 | 70518335200 | 100 POUCH in 1 BOX (70518-3352-0) > 1 CAPSULE in 1 POUCH (70518-3352-1) | 100 pouch | 2022-01-31 | 0000-00-00 | No | No | Current |