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"47335-322-88" National Drug Code (NDC)
Memantine Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (47335-322-88)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-322-88
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (47335-322-88)
Product NDC
47335-322
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Memantine Hydrochloride
Non-Proprietary Name
Memantine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150711
Marketing Category Name
ANDA
Application Number
ANDA090058
Manufacturer
Sun Pharmaceutical Industries, Inc.
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/47335-322-88