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"68382-735-77" National Drug Code (NDC)
Voriconazole 10 BLISTER PACK in 1 CARTON (68382-735-77) > 10 TABLET in 1 BLISTER PACK (68382-735-30)
(Zydus Pharmaceuticals (USA) Inc.)
NDC Code
68382-735-77
Package Description
10 BLISTER PACK in 1 CARTON (68382-735-77) > 10 TABLET in 1 BLISTER PACK (68382-735-30)
Product NDC
68382-735
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Voriconazole
Non-Proprietary Name
Voriconazole
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160525
End Marketing Date
20200801
Marketing Category Name
ANDA
Application Number
ANDA206747
Manufacturer
Zydus Pharmaceuticals (USA) Inc.
Substance Name
VORICONAZOLE
Strength
50
Strength Unit
mg/1
Pharmacy Classes
Azole Antifungal [EPC],Azoles [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-735-77