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"61919-371-20" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE (61919-371-20)
(Direct_Rx)

NDC Code61919-371-20
Package Description20 TABLET in 1 BOTTLE (61919-371-20)
Product NDC61919-371
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20190814
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerDirect_Rx
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-371-20





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