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"68071-2384-7" National Drug Code (NDC)

Ciprofloxacin 21 TABLET, COATED in 1 BOTTLE (68071-2384-7)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2384-7
Package Description21 TABLET, COATED in 1 BOTTLE (68071-2384-7)
Product NDC68071-2384
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20200812
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-2384-7





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