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"70518-1090-0" National Drug Code (NDC)
Ciprofloxacin 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1090-0)
(REMEDYREPACK INC.)
NDC Code
70518-1090-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1090-0)
Product NDC
70518-1090
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180402
Marketing Category Name
ANDA
Application Number
ANDA075593
Manufacturer
REMEDYREPACK 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/70518-1090-0