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Carbinoxamine Maleate - 51991-334-04 - (carbinoxamine maleate)

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Drug Information of Carbinoxamine Maleate

Product NDC: 51991-334
Proprietary Name: Carbinoxamine Maleate
Non Proprietary Name: carbinoxamine maleate
Active Ingredient(s): 4    mg/5mL & nbsp;   carbinoxamine maleate
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Carbinoxamine Maleate

Product NDC: 51991-334
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040458
Marketing Category: ANDA
Start Marketing Date: 20121210

Package Information of Carbinoxamine Maleate

Package NDC: 51991-334-04
Package Description: 118 mL in 1 BOTTLE, PLASTIC (51991-334-04)

NDC Information of Carbinoxamine Maleate

NDC Code 51991-334-04
Proprietary Name Carbinoxamine Maleate
Package Description 118 mL in 1 BOTTLE, PLASTIC (51991-334-04)
Product NDC 51991-334
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name carbinoxamine maleate
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20121210
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name CARBINOXAMINE MALEATE
Strength Number 4
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Carbinoxamine Maleate


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