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"47335-031-18" National Drug Code (NDC)
Memantine Hydrochloride 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-031-18)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
47335-031-18
Package Description
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-031-18)
Product NDC
47335-031
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Memantine Hydrochloride
Non-Proprietary Name
Memantine Hydrochloride
Dosage Form
CAPSULE, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20130614
Marketing Category Name
ANDA
Application Number
ANDA205905
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
MEMANTINE HYDROCHLORIDE
Strength
7
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/47335-031-18