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"70518-3417-2" National Drug Code (NDC)
Ciprofloxacin 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-2)
(REMEDYREPACK INC.)
NDC Code
70518-3417-2
Package Description
20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-2)
Product NDC
70518-3417
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20220511
Marketing Category Name
ANDA
Application Number
ANDA208921
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/70518-3417-2