memantine hydrochloride tablets

SPL v7

SPL

SPL Set ID 514421f3-f525-43e8-aecc-8b2bbffd00dc

Route

oral

Published

Effective Date 2024-08-16

Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients

memantine (5 mg)

Inactive Ingredients

silicon dioxide croscarmellose sodium dibasic calcium phosphate dihydrate hypromelloses cellulose, microcrystalline magnesium stearate povidone talc titanium dioxide polyethylene glycol, unspecified

Identifiers & Packaging

Pill Appearance

Imprint: ZF;40 Shape: capsule Color: white Size: 9 mm Size: 11 mm Score: 1

Marketing Status

anda active Since 2017-09-28

Description

NDC 70771-1119-5 in bottle of 500 tablets Memantine Hydrochloride Tablets USP, 5 mg Rx only 500 tablets NDC 70771-1120-5 in bottle of 500 tablets Memantine Hydrochloride Tablets USP, 10 mg Rx only 500 tablets

Medication Information

Description

Package Label.principal Display Panel

NDC 70771-1119-5 in bottle of 500 tablets

Memantine Hydrochloride Tablets USP, 5 mg

Rx only

500 tablets

NDC 70771-1120-5 in bottle of 500 tablets

Memantine Hydrochloride Tablets USP, 10 mg

Rx only

500 tablets

Structured Label Content

Package Label.principal Display Panel (PACKAGE LABEL.PRINCIPAL DISPLAY PANEL)

NDC 70771-1119-5 in bottle of 500 tablets

Memantine Hydrochloride Tablets USP, 5 mg

Rx only

500 tablets

NDC 70771-1120-5 in bottle of 500 tablets

Memantine Hydrochloride Tablets USP, 10 mg

Rx only

500 tablets

Advanced Ingredient Data

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Raw Label Data

All Sections (JSON)

{"PACKAGE LABEL.PRINCIPAL DISPLAY PANEL": "NDC 70771-1119-5 in bottle of 500 tablets Memantine Hydrochloride Tablets USP, 5 mg Rx only 500 tablets NDC 70771-1120-5 in bottle of 500 tablets Memantine Hydrochloride Tablets USP, 10 mg Rx only 500 tablets"}

Additional Information

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Source: dailymed · Ingested: 2026-02-15T11:42:31.680310 · Updated: 2026-03-14T22:09:49.950257