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"68071-2382-1" National Drug Code (NDC)

Ciprofloxacin 10 TABLET, FILM COATED in 1 BOTTLE (68071-2382-1)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2382-1
Package Description10 TABLET, FILM COATED in 1 BOTTLE (68071-2382-1)
Product NDC68071-2382
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070426
Marketing Category NameANDA
Application NumberANDA077859
ManufacturerNuCare Pharmaceuticals,Inc.
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/68071-2382-1





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