Phenoxybenzamine Hydrochloride
- Product NDC
- 0054-0349
- 11-digit product format
- 000540349
- Labeler code
- 0054
- Product ID
- 0054-0349_ccfdacba-c4d3-4977-8a7e-c265d0fe277a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenoxybenzamine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA201050
- Marketing category
- ANDA
- Marketing start
- 2015-08-10
- Marketing end
- 0000-00-00
- Substance
- PHENOXYBENZAMINE 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0054-0349-25 | 00054034925 | 100 CAPSULE in 1 BOTTLE (0054-0349-25) | 100 capsule | 2015-08-10 | 0000-00-00 | No | No | Current |