Phenoxybenzamine Hydrochloride is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Prasco Laboratories. The primary component is Phenoxybenzamine Hydrochloride.
Product ID | 66993-066_10386e7a-44ef-4bab-ba57-a11790bb1a6b |
NDC | 66993-066 |
Product Type | Human Prescription Drug |
Proprietary Name | Phenoxybenzamine Hydrochloride |
Generic Name | Phenoxybenzamine Hydrochloride |
Dosage Form | Capsule |
Route of Administration | ORAL |
Marketing Start Date | 2015-08-11 |
Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
Application Number | NDA008708 |
Labeler Name | Prasco Laboratories |
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 | 2020-12-31 |
Marketing Start Date | 2015-08-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA008708 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2015-08-11 |
Ingredient | Strength |
---|---|
PHENOXYBENZAMINE HYDROCHLORIDE | 10 mg/1 |
SPL SET ID: | 29ddb739-0f8e-4c41-ab4b-a6331ae2d508 |
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 |