Namenda Xr

Active Ingredient(s): Memantine Hydrochloride
FDA Approved: * June 21, 2010
Pharm Company: * FOREST LABS
Category: Alzheimers / Dementia

Memantine is a medication used to slow the progression of moderate-to-severe Alzheimer's disease.[2][3] It is taken by mouth.[2] Common side effects include headache, constipation, sleepiness, and dizziness.[2][3] Severe side effects may include blood clots, psychosis, and heart failure.[3] It is believed to work by blocking NMDA receptors.[2] Memantine was approved for medical use ... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
1 Discussion

Dosage List

Namenda Xr FLI;7;mg
24 Hr Namenda 7 mg Extended Release Capsule
NDC: 0456-3407
Labeler:
Forest Laboratories, Inc.
Namenda Xr FLI;28;mg
24 Hr Namenda 28 mg Extended Release Capsule
NDC: 0456-3428
Labeler:
Forest Laboratories, Inc.
Namenda Xr FLI;28;mg
Namenda 28 mg Oral Capsule, Extended Release
NDC: 68151-5817
Labeler:
Carilion Materials Management
Namenda Xr FLI;28;mg
Namenda 28 mg Oral Capsule, Extended Release
NDC: 68151-5829
Labeler:
Carilion Materials Management
Namenda Xr FLI;7;mg
Namenda 7 mg Oral Capsule, Extended Release
NDC: 69189-3407
Labeler:
Avera Mckennan Hospital
Namenda Xr FLI;28;mg
Namenda 28 mg Oral Capsule, Extended Release
NDC: 69189-3428
Labeler:
Avera Mckennan Hospital
Namenda 28 Day Titration Pack
NDC: 0456-3400
Labeler:
Forest Laboratories, Inc.
24 Hr Namenda 14 mg Extended Release Capsule
NDC: 0456-3414
Labeler:
Forest Laboratories, Inc.
24 Hr Namenda 21 mg Extended Release Capsule
NDC: 0456-3421
Labeler:
Forest Laboratories, Inc.
Namenda 14 mg Oral Capsule, Extended Release
NDC: 68151-5755
Labeler:
Carilion Materials Management

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