Prazosin Hydrochloride
- Product NDC
- 50090-1948
- 11-digit product format
- 500901948
- Labeler code
- 50090
- Product ID
- 50090-1948_eac2e002-5885-429a-9cd9-4c5402624fab
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 1989-02-28
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1948-1 | 50090194801 | 30 CAPSULE in 1 BOTTLE (50090-1948-1) | 30 capsule | 2015-08-10 | 0000-00-00 | No | No | Current |