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"16781-201-96" National Drug Code (NDC)
Benzefoam Ultra 1 CAN in 1 CARTON (16781-201-96) > 100 g in 1 CAN
(Onset Dermatologics LLC)
NDC Code
16781-201-96
Package Description
1 CAN in 1 CARTON (16781-201-96) > 100 g in 1 CAN
Product NDC
16781-201
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benzefoam Ultra
Non-Proprietary Name
Benzoyl Peroxide
Dosage Form
AEROSOL, FOAM
Usage
TOPICAL
Start Marketing Date
20110304
Marketing Category Name
UNAPPROVED DRUG OTHER
Manufacturer
Onset Dermatologics LLC
Substance Name
BENZOYL PEROXIDE
Strength
9.8
Strength Unit
g/100g
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16781-201-96