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NDC 70518-3338-00 Memantine Hydrochloride 5 mg/1 Details

Memantine Hydrochloride 5 mg/1

Memantine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is MEMANTINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Memantine is used to treat the symptoms of Alzheimer's disease (AD; a brain disease that slowly destroys the memory and the ability to think, learn, communicate and handle daily activities). Memantine is in a class of medications called NMDA receptor antagonists. It works by decreasing abnormal activity in the brain. Memantine may improve the ability to think and remember or may slow the loss of these abilities in people who have AD. However, memantine will not cure AD or prevent the loss of these abilities at some time in the future.

Related Packages: 70518-3338-00
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Memantine

Product Information

NDC	70518-3338
Product ID	70518-3338_06c24116-7195-9803-e063-6294a90ac79d
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Memantine Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Memantine Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	5
Active Ingredient Units	mg/1
Substance Name	MEMANTINE HYDROCHLORIDE
Labeler Name	REMEDYREPACK INC.
Pharmaceutical Class	N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA090961
Listing Certified Through	2024-12-31

Package

NDC 70518-3338-00 (70518333800)

Pricing Information	N/A
NDC Package Code	70518-3338-0
Billing NDC	70518333800
Package	30 TABLET in 1 BOTTLE, PLASTIC (70518-3338-0)
Marketing Start Date	2022-01-20
NDC Exclude Flag	N