Prazosin Hydrochloride
- Product NDC
- 63629-8325
- 11-digit product format
- 636298325
- Labeler code
- 63629
- Product ID
- 63629-8325_c76d3970-170b-41de-ba7f-3bdde4229325
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210971
- Marketing category
- ANDA
- Marketing start
- 2018-10-03
- 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 |
|---|
| 63629-8325-1 | 63629832501 | 60 CAPSULE in 1 BOTTLE (63629-8325-1) | 60 capsule | 2020-06-10 | 0000-00-00 | No | No | Current |
| 63629-8325-2 | 63629832502 | 30 CAPSULE in 1 BOTTLE (63629-8325-2) | 30 capsule | 2021-12-23 | 0000-00-00 | No | No | Current |