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"0093-4742-05" National Drug Code (NDC)

Citalopram 500 TABLET in 1 BOTTLE (0093-4742-05)
(Teva Pharmaceuticals USA Inc)

NDC Code0093-4742-05
Package Description500 TABLET in 1 BOTTLE (0093-4742-05)
Product NDC0093-4742
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCitalopram
Non-Proprietary NameCitalopram
Dosage FormTABLET
UsageORAL
Start Marketing Date20071108
End Marketing Date20160331
Marketing Category NameANDA
Application NumberANDA077048
ManufacturerTeva Pharmaceuticals USA Inc
Substance NameCITALOPRAM HYDROBROMIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-4742-05





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