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Benzoyl Peroxide - 68462-412-38 - (Benzoyl Peroxide)

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Drug Information of Benzoyl Peroxide

Product NDC: 68462-412
Proprietary Name: Benzoyl Peroxide
Non Proprietary Name: Benzoyl Peroxide
Active Ingredient(s): 6    g/100mL & nbsp;   Benzoyl Peroxide
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Benzoyl Peroxide

Product NDC: 68462-412
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090320

Package Information of Benzoyl Peroxide

Package NDC: 68462-412-38
Package Description: 177.4 mL in 1 TUBE (68462-412-38)

NDC Information of Benzoyl Peroxide

NDC Code 68462-412-38
Proprietary Name Benzoyl Peroxide
Package Description 177.4 mL in 1 TUBE (68462-412-38)
Product NDC 68462-412
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benzoyl Peroxide
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20090320
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Glenmark Generics Inc., USA
Substance Name BENZOYL PEROXIDE
Strength Number 6
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Benzoyl Peroxide


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