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"68071-2391-3" National Drug Code (NDC)
Ciprofloxacin 30 TABLET, FILM COATED in 1 BOTTLE (68071-2391-3)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-2391-3
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (68071-2391-3)
Product NDC
68071-2391
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20040609
Marketing Category Name
ANDA
Application Number
ANDA075593
Manufacturer
NuCare Pharmaceuticals,Inc.
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Quinolone Antimicrobial [EPC], Quinolones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-2391-3