Phenoxybenzamine Hydrochloride is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Hikma Pharmaceuticals Usa Inc.. The primary component is Phenoxybenzamine Hydrochloride.
| Product ID | 0054-0349_ccfdacba-c4d3-4977-8a7e-c265d0fe277a | 
| NDC | 0054-0349 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Phenoxybenzamine Hydrochloride | 
| Generic Name | Phenoxybenzamine Hydrochloride | 
| Dosage Form | Capsule | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2015-08-10 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA201050 | 
| Labeler Name | Hikma Pharmaceuticals USA Inc. | 
| Substance Name | PHENOXYBENZAMINE HYDROCHLORIDE | 
| Active Ingredient Strength | 10 mg/1 | 
| Pharm Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2021-12-31 | 
| Marketing Start Date | 2015-08-10 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA201050 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2015-08-10 | 
| Ingredient | Strength | 
|---|---|
| PHENOXYBENZAMINE HYDROCHLORIDE | 10 mg/1 | 
| SPL SET ID: | 79a53bb1-fa5a-41a7-aeaf-01a60fb4f810 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0054-0349 | Phenoxybenzamine Hydrochloride | Phenoxybenzamine Hydrochloride | 
| 49884-038 | Phenoxybenzamine Hydrochloride | Phenoxybenzamine Hydrochloride | 
| 60219-1502 | Phenoxybenzamine hydrochloride | Phenoxybenzamine hydrochloride | 
| 66993-066 | Phenoxybenzamine Hydrochloride | Phenoxybenzamine Hydrochloride | 
| 69238-1502 | Phenoxybenzamine hydrochloride | Phenoxybenzamine hydrochloride | 
| 70954-365 | Phenoxybenzamine Hydrochloride | Phenoxybenzamine Hydrochloride | 
| 59212-001 | Dibenzyline | Phenoxybenzamine Hydrochloride |