"72603-119-02" National Drug Code (NDC)

Memantine 500 TABLET in 1 BOTTLE (72603-119-02)
(NorthStar RxLLC)

NDC Code72603-119-02
Package Description500 TABLET in 1 BOTTLE (72603-119-02)
Product NDC72603-119
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMemantine
Non-Proprietary NameMemantine
Dosage FormTABLET
UsageORAL
Start Marketing Date20220913
Marketing Category NameANDA
Application NumberANDA090048
ManufacturerNorthStar RxLLC
Substance NameMEMANTINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesN-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]

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