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"69097-822-12" National Drug Code (NDC)

Citalopram 500 TABLET in 1 BOTTLE (69097-822-12)
(Cipla USA Inc.)

NDC Code69097-822-12
Package Description500 TABLET in 1 BOTTLE (69097-822-12)
Product NDC69097-822
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCitalopram
Non-Proprietary NameCitalopram
Dosage FormTABLET
UsageORAL
Start Marketing Date20160722
Marketing Category NameANDA
Application NumberANDA077534
ManufacturerCipla USA Inc.
Substance NameCITALOPRAM HYDROBROMIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSerotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69097-822-12





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