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"68071-1893-2" National Drug Code (NDC)
Ciprofloxacin 21 TABLET in 1 BOTTLE (68071-1893-2)
(NuCare Pharmaceuticals, Inc.)
NDC Code
68071-1893-2
Package Description
21 TABLET in 1 BOTTLE (68071-1893-2)
Product NDC
68071-1893
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20040910
Marketing Category Name
ANDA
Application Number
ANDA076639
Manufacturer
NuCare Pharmaceuticals, Inc.
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Quinolone Antimicrobial [EPC], Quinolones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68071-1893-2