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"62032-415-20" National Drug Code (NDC)
Tretinoin 1 TUBE in 1 CARTON (62032-415-20) > 20 g in 1 TUBE
(OMP, INC.)
NDC Code
62032-415-20
Package Description
1 TUBE in 1 CARTON (62032-415-20) > 20 g in 1 TUBE
Product NDC
62032-415
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tretinoin
Non-Proprietary Name
Tretinoin
Dosage Form
CREAM
Usage
TOPICAL
Start Marketing Date
20131001
End Marketing Date
20160831
Marketing Category Name
ANDA
Application Number
ANDA075265
Manufacturer
OMP, INC.
Substance Name
TRETINOIN
Strength
.5
Strength Unit
mg/g
Pharmacy Classes
Retinoid [EPC],Retinoids [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/62032-415-20