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"62032-413-20" National Drug Code (NDC)
Tretinoin 20 g in 1 TUBE (62032-413-20)
(Obagi Cosmeceuticals LLC)
NDC Code
62032-413-20
Package Description
20 g in 1 TUBE (62032-413-20)
Product NDC
62032-413
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tretinoin
Non-Proprietary Name
Tretinoin
Dosage Form
GEL
Usage
TOPICAL
Start Marketing Date
20140619
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA022070
Manufacturer
Obagi Cosmeceuticals LLC
Substance Name
TRETINOIN
Strength
.05
Strength Unit
g/100g
Pharmacy Classes
Retinoid [EPC], Retinoids [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/62032-413-20