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"70518-4172-0" National Drug Code (NDC)

Tindazole 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4172-0)
(REMEDYREPACK INC.)

NDC Code70518-4172-0
Package Description8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4172-0)
Product NDC70518-4172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTindazole
Non-Proprietary NameTinidazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240830
Marketing Category NameANDA
Application NumberANDA202489
ManufacturerREMEDYREPACK INC.
Substance NameTINIDAZOLE
Strength500
Strength Unitmg/1
Pharmacy ClassesNitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-4172-0





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