Prazosin Hydrochloride
- Product NDC
- 68071-2713
- 11-digit product format
- 680712713
- Labeler code
- 68071
- Product ID
- 68071-2713_df7434aa-d4c3-63a1-e053-2a95a90a2751
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA210971
- Marketing category
- ANDA
- Marketing start
- 2018-10-03
- Marketing end
- 0000-00-00
- Substance
- PRAZOSIN HYDROCHLORIDE
- Active strength
- 1 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
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 |
|---|
| 68071-2713-9 | Prazosin Hydrochloride | 90 in 1 BOTTLE | CAPSULE | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2713 | PRAZOSIN HYDROCHLORIDE CAPSULE [NUCARE PHARMACEUTICALS,INC.] | 1 | Legacy NDC, 1 package rows | 20220521_df7434aa-d4c2-63a1-e053-2a95a90a2751.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 |
|---|
| 68071-2713-9 | 68071271309 | 90 CAPSULE in 1 BOTTLE (68071-2713-9) | 90 capsule | 2022-05-20 | 0000-00-00 | No | No | Current |