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"72603-119-02" National Drug Code (NDC)
Memantine 500 TABLET in 1 BOTTLE (72603-119-02)
(NorthStar RxLLC)
NDC Code
72603-119-02
Package Description
500 TABLET in 1 BOTTLE (72603-119-02)
Product NDC
72603-119
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Memantine
Non-Proprietary Name
Memantine
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220913
Marketing Category Name
ANDA
Application Number
ANDA090048
Manufacturer
NorthStar RxLLC
Substance Name
MEMANTINE HYDROCHLORIDE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72603-119-02