Alfuzosin Hydrochloride
- Product NDC
- 63629-2353
- 11-digit product format
- 636292353
- Labeler code
- 63629
- Product ID
- 63629-2353_eec05448-affa-4bae-a4fd-ee2334f77474
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alfuzosin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079057
- Marketing category
- ANDA
- Marketing start
- 2011-11-22
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2353-1 | 63629235301 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2353-1) | 2021-02-18 | 0000-00-00 | No | No | Current |