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"71335-2952-1" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (71335-2952-1) / 45 g in 1 TUBE
(Bryant Ranch Prepack)

NDC Code71335-2952-1
Package Description1 TUBE in 1 CARTON (71335-2952-1) / 45 g in 1 TUBE
Product NDC71335-2952
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2952-1





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