"63323-738-04" National Drug Code (NDC)

Famotidine 1 VIAL, MULTI-DOSE in 1 CARTON (63323-738-04) > 4 mL in 1 VIAL, MULTI-DOSE
(Fresenius Kabi USA, LLC)

NDC Code63323-738-04
Package Description1 VIAL, MULTI-DOSE in 1 CARTON (63323-738-04) > 4 mL in 1 VIAL, MULTI-DOSE
Product NDC63323-738
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormINJECTION, SOLUTION
UsageINTRAVENOUS
Start Marketing Date20010719
Marketing Category NameANDA
Application NumberANDA075709
ManufacturerFresenius Kabi USA, LLC
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/mL
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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