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"72789-519-10" National Drug Code (NDC)
Ciprofloxacin 10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10)
(PD-Rx Pharmaceuticals, Inc.)
NDC Code
72789-519-10
Package Description
10 TABLET in 1 BOTTLE, PLASTIC (72789-519-10)
Product NDC
72789-519
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Ciprofloxacin
Non-Proprietary Name
Ciprofolxacin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20231001
Marketing Category Name
ANDA
Application Number
ANDA208921
Manufacturer
PD-Rx Pharmaceuticals, 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/72789-519-10