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"50436-3135-4" National Drug Code (NDC)
Ciprofloxacin 10 TABLET in 1 BOTTLE (50436-3135-4)
(Unit Dose Services)
NDC Code
50436-3135-4
Package Description
10 TABLET in 1 BOTTLE (50436-3135-4)
Product NDC
50436-3135
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
Unit Dose Services
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/50436-3135-4