Arbinoxa - 63717-870-01 - (Carbinoxamine Maleate)

Alphabetical Index


Drug Information of Arbinoxa

Product NDC: 63717-870
Proprietary Name: Arbinoxa
Non Proprietary Name: Carbinoxamine Maleate
Active Ingredient(s): 4    mg/1 & nbsp;   Carbinoxamine Maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Arbinoxa

Product NDC: 63717-870
Labeler Name: Hawthorn Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090417
Marketing Category: ANDA
Start Marketing Date: 20100823

Package Information of Arbinoxa

Package NDC: 63717-870-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (63717-870-01)

NDC Information of Arbinoxa

NDC Code 63717-870-01
Proprietary Name Arbinoxa
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (63717-870-01)
Product NDC 63717-870
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbinoxamine Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100823
Marketing Category Name ANDA
Labeler Name Hawthorn Pharmaceuticals, Inc.
Substance Name CARBINOXAMINE MALEATE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Arbinoxa


General Information