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"47335-322-13" National Drug Code (NDC)

Memantine Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (47335-322-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-322-13
Package Description500 TABLET, FILM COATED in 1 BOTTLE (47335-322-13)
Product NDC47335-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMemantine Hydrochloride
Non-Proprietary NameMemantine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150711
Marketing Category NameANDA
Application NumberANDA090058
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameMEMANTINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesN-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/47335-322-13





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