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"70436-230-39" National Drug Code (NDC)

Voriconazole 1 BOTTLE in 1 CARTON (70436-230-39) / 75 mL in 1 BOTTLE
(Slate Run Pharmaceuticals, LLC)

NDC Code70436-230-39
Package Description1 BOTTLE in 1 CARTON (70436-230-39) / 75 mL in 1 BOTTLE
Product NDC70436-230
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameVoriconazole
Non-Proprietary NameVoriconazole
Dosage FormPOWDER, FOR SUSPENSION
UsageORAL
Start Marketing Date20240501
Marketing Category NameANDA
Application NumberANDA216805
ManufacturerSlate Run Pharmaceuticals, LLC
Substance NameVORICONAZOLE
Strength40
Strength Unitmg/mL
Pharmacy ClassesAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70436-230-39





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