Prazosin Hydrochloride
- Product NDC
- 68788-7824
- 11-digit product format
- 687887824
- Labeler code
- 68788
- Product ID
- 68788-7824_7111161f-3a9c-4c64-80a9-80f419f4dcbe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- P)referred Pharmaceuticals Inc.
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2021-01-05
- 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 |
|---|
| 68788-7824-1 | 68788782401 | 100 CAPSULE in 1 BOTTLE (68788-7824-1) | 100 capsule | 2021-01-05 | 0000-00-00 | No | No | Current |
| 68788-7824-3 | 68788782403 | 30 CAPSULE in 1 BOTTLE (68788-7824-3) | 30 capsule | 2021-01-05 | 0000-00-00 | No | No | Current |
| 68788-7824-6 | 68788782406 | 60 CAPSULE in 1 BOTTLE (68788-7824-6) | 60 capsule | 2021-01-05 | 0000-00-00 | No | No | Current |
| 68788-7824-9 | 68788782409 | 90 CAPSULE in 1 BOTTLE (68788-7824-9) | 90 capsule | 2021-01-05 | 0000-00-00 | No | No | Current |