"24208-535-32" National Drug Code (NDC)

Zirgan 1 TUBE, WITH APPLICATOR in 1 CARTON (24208-535-32) > 1 g in 1 TUBE, WITH APPLICATOR
(Bausch & Lomb Incorporated)

NDC Code24208-535-32
Package Description1 TUBE, WITH APPLICATOR in 1 CARTON (24208-535-32) > 1 g in 1 TUBE, WITH APPLICATOR
Product NDC24208-535
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZirgan
Non-Proprietary NameGanciclovir
Dosage FormGEL
UsageOPHTHALMIC
Start Marketing Date20100430
Marketing Category NameNDA
Application NumberNDA022211
ManufacturerBausch & Lomb Incorporated
Substance NameGANCICLOVIR
Strength1.5
Strength Unitmg/g
Pharmacy ClassesCytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC]

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