Prazosin Hydrochloride
- Product NDC
- 70518-1476
- 11-digit product format
- 705181476
- Labeler code
- 70518
- Product ID
- 70518-1476_93358158-cfec-4f7f-e053-2995a90a4452
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prazosin hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA072575
- Marketing category
- ANDA
- Marketing start
- 2018-10-06
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1476 | PRAZOSIN HYDROCHLORIDE CAPSULE [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250125_fece0532-2c89-4f09-b5a5-34c808d09224.zip |