"68071-3889-2" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (68071-3889-2) / 20 g in 1 TUBE
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-3889-2
Package Description1 TUBE in 1 CARTON (68071-3889-2) / 20 g in 1 TUBE
Product NDC68071-3889
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20190122
Marketing Category NameANDA
Application NumberANDA211645
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameTRETINOIN
Strength1
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

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