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"72189-111-30" National Drug Code (NDC)
Ciprofloxacin 30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)
(DIRECT RX)
NDC Code
72189-111-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-111-30)
Product NDC
72189-111
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofloxacin Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20200612
Marketing Category Name
ANDA
Application Number
ANDA077859
Manufacturer
DIRECT RX
Substance Name
CIPROFLOXACIN HYDROCHLORIDE
Strength
500
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/72189-111-30