PRAZOSIN HYDROCHLORIDE
- Product NDC
- 61919-910
- 11-digit product format
- 619190910
- Labeler code
- 61919
- Product ID
- 61919-910_94f330c0-5091-6d12-e053-2995a90a0991
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAZOSIN HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA071745
- Marketing category
- ANDA
- Marketing start
- 2018-03-12
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-910-60 | PRAZOSIN HYDROCHLORIDE | 60 in 1 BOTTLE | CAPSULE | 60 | | 2 |
| 61919-910-90 | PRAZOSIN HYDROCHLORIDE | 90 in 1 BOTTLE | CAPSULE | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-910 | PRAZOSIN HYDROCHLORIDE CAPSULE [DIRECT RX] | 2 | Legacy NDC, 2 package rows | 20191016_673ca980-7d1c-2517-e053-2991aa0ad2d6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-910-60 | 61919091060 | 60 CAPSULE in 1 BOTTLE (61919-910-60) | 60 capsule | 2018-03-12 | 0000-00-00 | No | No | Current |
| 61919-910-90 | 61919091090 | 90 CAPSULE in 1 BOTTLE (61919-910-90) | 90 capsule | 2018-03-12 | 0000-00-00 | No | No | Current |