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"72162-2135-2" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (72162-2135-2) / 20 g in 1 TUBE
(Bryant Ranch Prepack)

NDC Code72162-2135-2
Package Description1 TUBE in 1 CARTON (72162-2135-2) / 20 g in 1 TUBE
Product NDC72162-2135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20170615
Marketing Category NameANDA
Application NumberANDA075264
ManufacturerBryant Ranch Prepack
Substance NameTRETINOIN
Strength.25
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72162-2135-2





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