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"70518-3223-0" National Drug Code (NDC)

Tretinoin 1 TUBE in 1 CARTON (70518-3223-0) / 20 g in 1 TUBE
(REMEDYREPACK INC.)

NDC Code70518-3223-0
Package Description1 TUBE in 1 CARTON (70518-3223-0) / 20 g in 1 TUBE
Product NDC70518-3223
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTretinoin
Non-Proprietary NameTretinoin
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20210914
Marketing Category NameANDA
Application NumberANDA211645
ManufacturerREMEDYREPACK INC.
Substance NameTRETINOIN
Strength1
Strength Unitmg/g
Pharmacy ClassesRetinoid [EPC], Retinoids [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3223-0





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