ALFUZOSIN HYDROCHLORIDE
- Product NDC
- 61919-349
- 11-digit product format
- 619190349
- Labeler code
- 61919
- Product ID
- 61919-349_9c59151b-2a77-a008-e053-2a95a90a70d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALFUZOSIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA079057
- Marketing category
- ANDA
- Marketing start
- 2015-12-21
- Marketing end
- 0000-00-00
- Substance
- ALFUZOSIN HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-349-30 | ALFUZOSIN HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-349 | ALFUZOSIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [DIRECTRX] | 2 | Legacy NDC, 1 package rows | 20200129_27f6bec9-90a9-4c4c-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-349-30 | 61919034930 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-349-30) | 2015-12-21 | 0000-00-00 | No | No | Current |