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"71717-101-03" National Drug Code (NDC)
Clopidogrel 30 TABLET in 1 BOTTLE, PLASTIC (71717-101-03)
(Megalith Pharmaceuticals Inc)
NDC Code
71717-101-03
Package Description
30 TABLET in 1 BOTTLE, PLASTIC (71717-101-03)
Product NDC
71717-101
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Clopidogrel
Non-Proprietary Name
Clopidogrel
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20171201
Marketing Category Name
ANDA
Application Number
ANDA204359
Manufacturer
Megalith Pharmaceuticals Inc
Substance Name
CLOPIDOGREL BISULFATE
Strength
75
Strength Unit
mg/1
Pharmacy Classes
Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71717-101-03