Minipress
- Product NDC
- 0069-4310
- 11-digit product format
- 000694310
- Labeler code
- 0069
- Product ID
- 0069-4310_23047548-9790-4916-82c0-af04fed6be95
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Application
- NDA017442
- Marketing category
- NDA
- Marketing start
- 1994-05-10
- 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
- 2022-12-31
- 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 |
|---|
| 0069-4310-71 | 00069431071 | 250 CAPSULE in 1 BOTTLE (0069-4310-71) | 250 capsule | 1994-05-10 | 0000-00-00 | No | No | Current |