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"21695-210-14" National Drug Code (NDC)
Ciprofloxacin 14 TABLET, FILM COATED in 1 BOTTLE (21695-210-14)
(Rebel Distributors Corp.)
NDC Code
21695-210-14
Package Description
14 TABLET, FILM COATED in 1 BOTTLE (21695-210-14)
Product NDC
21695-210
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20040609
Marketing Category Name
ANDA
Application Number
ANDA076794
Manufacturer
Rebel Distributors Corp.
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/21695-210-14