Prazosin Hydrochloride
- Product NDC
- 64725-4067
- 11-digit product format
- 647254067
- Labeler code
- 64725
- Product ID
- 64725-4067_782770e7-b6bd-4ed0-b7b7-99efc7b392cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prazosin Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA071994
- Marketing category
- ANDA
- Marketing start
- 2007-02-22
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 64725-4067-1 | Prazosin Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-4067 | PRAZOSIN HYDROCHLORIDE CAPSULE [TYA PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20141110_c6409bb4-59fc-4f46-80b3-a2b2ac654350.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-4067-1 | 64725406701 | 100 in 1 BOTTLE | Historical |