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Carbinoxamine Maleate - 64376-605-01 - (Carbinoxamine Maleate)

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Drug Information of Carbinoxamine Maleate

Product NDC: 64376-605
Proprietary Name: Carbinoxamine Maleate
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 Carbinoxamine Maleate

Product NDC: 64376-605
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040639
Marketing Category: ANDA
Start Marketing Date: 20080530

Package Information of Carbinoxamine Maleate

Package NDC: 64376-605-01
Package Description: 100 TABLET in 1 BOTTLE (64376-605-01)

NDC Information of Carbinoxamine Maleate

NDC Code 64376-605-01
Proprietary Name Carbinoxamine Maleate
Package Description 100 TABLET in 1 BOTTLE (64376-605-01)
Product NDC 64376-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Carbinoxamine Maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080530
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, Inc.
Substance Name CARBINOXAMINE MALEATE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Carbinoxamine Maleate


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