"72162-1071-2" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (72162-1071-2) / 45 g in 1 TUBE
(Bryant Ranch Prepack)

NDC Code72162-1071-2
Package Description1 TUBE in 1 CARTON (72162-1071-2) / 45 g in 1 TUBE
Product NDC72162-1071
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormGEL
UsageTOPICAL
Start Marketing Date20190812
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA017955
ManufacturerBryant Ranch Prepack
Substance NameTRETINOIN
Strength.1
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

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