Prazosin Hydrochloride
- Product NDC
- 71335-1556
- 11-digit product format
- 713351556
- Labeler code
- 71335
- Product ID
- 71335-1556_c1de956d-c6a7-44a4-a1d9-2cf7893644d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 1989-02-28
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 2 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 |
|---|
| 71335-1556-1 | 71335155601 | 30 CAPSULE in 1 BOTTLE (71335-1556-1) | 30 capsule | 2020-04-03 | 0000-00-00 | No | No | Current |
| 71335-1556-2 | 71335155602 | 28 CAPSULE in 1 BOTTLE (71335-1556-2) | 28 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-1556-3 | 71335155603 | 60 CAPSULE in 1 BOTTLE (71335-1556-3) | 60 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-1556-4 | 71335155604 | 90 CAPSULE in 1 BOTTLE (71335-1556-4) | 90 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |
| 71335-1556-5 | 71335155605 | 18 CAPSULE in 1 BOTTLE (71335-1556-5) | 18 capsule | 2022-05-02 | 0000-00-00 | No | No | Current |