"62032-415-20" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (62032-415-20) > 20 g in 1 TUBE
(OMP, INC.)

NDC Code62032-415-20
Package Description1 TUBE in 1 CARTON (62032-415-20) > 20 g in 1 TUBE
Product NDC62032-415
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20131001
End Marketing Date20160831
Marketing Category NameANDA
Application NumberANDA075265
ManufacturerOMP, INC.
Substance NameTRETINOIN
Strength.5
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC],Retinoids [Chemical/Ingredient]

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