Prazosin Hydrochloride
- Product NDC
- 68788-7447
- 11-digit product format
- 687887447
- Labeler code
- 68788
- Product ID
- 68788-7447_3feada6b-acf7-413b-b3f2-37d9ee617f53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA210971
- Marketing category
- ANDA
- Marketing start
- 2019-12-27
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- alpha-Adrenergic Blocker [EPC],Adrenergic alpha-Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 68788-7447-1 | 68788744701 | 100 CAPSULE in 1 BOTTLE (68788-7447-1) | 100 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7447-3 | 68788744703 | 30 CAPSULE in 1 BOTTLE (68788-7447-3) | 30 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7447-6 | 68788744706 | 60 CAPSULE in 1 BOTTLE (68788-7447-6) | 60 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7447-9 | 68788744709 | 90 CAPSULE in 1 BOTTLE (68788-7447-9) | 90 capsule | 2019-12-27 | 0000-00-00 | No | No | Current |