Phenoxybenzamine Hydrochloride
Phenoxybenzamine Hydrochloride Capsules, USP 10 mg adrenergic, -receptor-blocking agent
Approved
Approval ID
037202a5-e08b-4f9d-9df8-a6dd25027748
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 27, 2017
Manufacturers
FDA
Par Pharmaceutical, Inc.
DUNS: 092733690
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Phenoxybenzamine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code49884-038
Application NumberANDA204522
Product Classification
M
Marketing Category
C73584
G
Generic Name
Phenoxybenzamine Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateNovember 27, 2017
FDA Product Classification
INGREDIENTS (3)
PHENOXYBENZAMINE HYDROCHLORIDEActive
Quantity: 10 mg in 1 1
Code: X1IEG24OHL
Classification: ACTIB
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT