ALFUZOSIN HYDROCHLORIDE
- Product NDC
- 13668-021
- 11-digit product format
- 136680021
- Labeler code
- 13668
- Product ID
- 13668-021_bb8a401b-7a05-6e7f-e053-2995a90a8250
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALFUZOSIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Torrent Pharmaceuticals Limited
- Application
- ANDA079054
- Marketing category
- ANDA
- Marketing start
- 2011-07-18
- 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
- 2022-12-31
- 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 |
|---|
| 13668-021-01 | 13668002101 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-021-01) | 2011-07-18 | 0000-00-00 | No | No | Current |
| 13668-021-05 | 13668002105 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-021-05) | 2011-07-18 | 0000-00-00 | No | No | Current |
| 13668-021-30 | 13668002130 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (13668-021-30) | 2011-07-18 | 0000-00-00 | No | No | Current |
| 13668-021-64 | 13668002164 | 90 TABLET, EXTENDED RELEASE in 1 DOSE PACK (13668-021-64) | 2011-07-18 | 0000-00-00 | No | No | Current |