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"52125-069-02" National Drug Code (NDC)
Ciprofloxacin 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-069-02)
(REMEDYREPACK INC.)
NDC Code
52125-069-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (52125-069-02)
Product NDC
52125-069
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20130314
Marketing Category Name
ANDA
Application Number
ANDA076558
Manufacturer
REMEDYREPACK INC.
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-069-02