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"72789-233-10" National Drug Code (NDC)
Moxifloxacin 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)
(PD-Rx Pharmaceuticals, Inc.)
NDC Code
72789-233-10
Package Description
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10)
Product NDC
72789-233
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Moxifloxacin
Non-Proprietary Name
Moxifloxacin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140305
Marketing Category Name
ANDA
Application Number
ANDA076938
Manufacturer
PD-Rx Pharmaceuticals, Inc.
Substance Name
MOXIFLOXACIN HYDROCHLORIDE
Strength
400
Strength Unit
mg/1
Pharmacy Classes
Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72789-233-10