Drugplain

Donepezil Hydrochloride 5 mg/1

Donepezil Hydrochloride · TABLET · Bryant Ranch Prepack

1 Recall on Record
Plain English

Donepezil hydrochloride is a prescription tablet used to treat symptoms of Alzheimer's disease by helping to preserve acetylcholine in the brain. This medication is taken by mouth and may help improve memory and thinking ability in people with mild to moderate Alzheimer's disease.

Key Facts

Brand Name
Donepezil Hydrochloride
Generic Name
Donepezil Hydrochloride
NDC Code (Product)
71335-2065
Manufacturer
Bryant Ranch Prepack
Strength
5 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA078662
Marketing Start
06/29/2021

Recall History

1 Recall on Record
Class III12/13/2016

Sandoz Inc

Subpotent Drug: out of specification results for assay test.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

fall383 reports
fatigue271 reports
dizziness262 reports
diarrhoea259 reports
death241 reports
drug interaction224 reports
nausea221 reports
decreased appetite189 reports
asthenia188 reports
dyspnoea184 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE Donepezil hydrochloride tablet is an acetylcholinesterase inhibitor indicated for the treatment of dementia of the Alzheimer's type. Efficacy has been demonstrated in patients with mild, moderate, and severe Alzheimer's Disease ( 1 ). Donepezil hydrochloride tablet is indicated for the treatment of dementia of the Alzheimer's type. Efficacy has been demonstrated in patients with mild, moderate, and severe Alzheimer's disease.

Dosage & Administration

2 DOSAGE AND ADMINISTRATION Mild to Moderate Alzheimer's Disease: 5 mg to 10 mg once daily ( 2.1 ) Moderate to Severe Alzheimer's Disease: 10 mg to 23 mg once daily ( 2.2 ) 2.1 Dosing in Mild to Moderate Alzheimer’s Disease The recommended starting dosage of donepezil hydrochloride tablet is 5 mg administered once per day in the evening, just prior to retiring. The maximum recommended dosage of donepezil hydrochloride tablets in patients with mild to moderate Alzheimer's disease is 10 mg per day. A dose of 10 mg should not be administered until patients have been on a daily dose of 5 mg for 4 to 6 weeks. 2.2 Dosing in Moderate to Severe Alzheimer’s Disease The recommended starting dosage of donepezil hydrochloride tablet is 5 mg administered once per day in the evening, just prior to retiring. The maximum recommended dosage of donepezil hydrochloride tablets in patients with moderate to severe Alzheimer's disease is 23 mg per day. A dose of 10 mg should not be administered until patients have been on a daily dose of 5 mg for 4 to 6 weeks. A dose of 23 mg per day should not be administered until patients have been on a daily dose of 10 mg for at least 3 months. 2.3 Administration In

Contraindications

4 CONTRAINDICATIONS Known hypersensitivity to donepezil hydrochloride or to piperidine derivatives ( 4 ) Donepezil hydrochloride is contraindicated in patients with known hypersensitivity to donepezil hydrochloride or to piperidine derivatives.

Drug Interactions

7 DRUG INTERACTIONS Cholinesterase inhibitors have the potential to interfere with the activity of anticholinergic medications ( 7.1 ). A synergistic effect may be expected with concomitant administration of succinylcholine, similar neuromuscular blocking agents, or cholinergic agonists ( 7.2 ). 7.1 Use with Anticholinergics Because of their mechanism of action, cholinesterase inhibitors have the potential to interfere with the activity of anticholinergic medications. 7.2 Use with Cholinomimetics and Other Cholinesterase Inhibitors A synergistic effect may be expected when cholinesterase inhibitors are given concurrently with succinylcholine, similar neuromuscular blocking agents, or cholinergic agonists such as bethanechol.

Adverse Reactions

6 ADVERSE REACTIONS Most common adverse reactions in clinical studies of donepezil hydrochloride are nausea, diarrhea, insomnia, vomiting, muscle cramps, fatigue, and anorexia ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Lupin Pharmaceuticals, Inc. at 1-800-399-2561 or FDA at 1-800-FDA-1088 or www.fda.gov/ medwatch . The following serious adverse reactions are described below and elsewhere in the labeling: Cardiovascular Conditions [ see Warnings and Precautions ( 5.2 ) ]. Nausea and Vomiting [ see Warnings and Precautions ( 5.3 ) ]. Peptic Ulcer Disease and GI Bleeding [ see Warnings and Precautions ( 5.4 ) ]. Weight Loss [ see Warnings and Precautions ( 5.5 ) ]. Genitourinary Conditions [ see Warnings and Precautions ( 5.6 ) ]. Neurological Conditions: Seizures [ see Warnings and Precautions ( 5.7 ) ]. Pulmonary Conditions [ see Warnings and Precautions ( 5.8 ) ]. 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. Donepezil hydroc

Frequently Asked Questions

What is Donepezil Hydrochloride used for?

Donepezil hydrochloride is a prescription tablet used to treat symptoms of Alzheimer's disease by helping to preserve acetylcholine in the brain. This medication is taken by mouth and may help improve memory and thinking ability in people with mild to moderate Alzheimer's disease.

Is Donepezil Hydrochloride a controlled substance?

Donepezil Hydrochloride is not classified as a controlled substance by the DEA.

What is the generic name for Donepezil Hydrochloride?

The generic name for Donepezil Hydrochloride is Donepezil Hydrochloride. There are 7 other brand versions of Donepezil Hydrochloride.

What is the NDC code for Donepezil Hydrochloride 5 mg/1?

The NDC (National Drug Code) for Donepezil Hydrochloride 5 mg/1 is 71335-2065, listed by Bryant Ranch Prepack.