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"70518-3714-0" National Drug Code (NDC)
Ciprofloxacin 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3714-0)
(REMEDYREPACK INC.)
NDC Code
70518-3714-0
Package Description
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3714-0)
Product NDC
70518-3714
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230412
Marketing Category Name
ANDA
Application Number
ANDA077859
Manufacturer
REMEDYREPACK INC.
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3714-0