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"70518-0797-0" National Drug Code (NDC)
Metronidazole 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0797-0)
(REMEDYREPACK INC.)
NDC Code
70518-0797-0
Package Description
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0797-0)
Product NDC
70518-0797
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Metronidazole
Non-Proprietary Name
Metronidazole
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20171018
Marketing Category Name
ANDA
Application Number
ANDA203458
Manufacturer
REMEDYREPACK INC.
Substance Name
METRONIDAZOLE
Strength
250
Strength Unit
mg/1
Pharmacy Classes
Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0797-0