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Chlorpheniramine Maleate - 10702-017-06 - (Chlorpheniramine Maleate)

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Drug Information of Chlorpheniramine Maleate

Product NDC: 10702-017
Proprietary Name: Chlorpheniramine Maleate
Non Proprietary Name: Chlorpheniramine Maleate
Active Ingredient(s): 12    mg/1 & nbsp;   Chlorpheniramine Maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Chlorpheniramine Maleate

Product NDC: 10702-017
Labeler Name: KVK-Tech, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA040829
Marketing Category: ANDA
Start Marketing Date: 20100615

Package Information of Chlorpheniramine Maleate

Package NDC: 10702-017-06
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10702-017-06)

NDC Information of Chlorpheniramine Maleate

NDC Code 10702-017-06
Proprietary Name Chlorpheniramine Maleate
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10702-017-06)
Product NDC 10702-017
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chlorpheniramine Maleate
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100615
Marketing Category Name ANDA
Labeler Name KVK-Tech, Inc.
Substance Name CHLORPHENIRAMINE MALEATE
Strength Number 12
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Chlorpheniramine Maleate


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