75929-087 : Aricept 23 mg Oral Tablet, Film Coated


NDC: 75929-087
Labeler: Pharma Packaging Solutions, LLC Dba Tjoapack LLC
Product Type: Human Prescription Drug
Drug Name:  Aricept
Dosage Form: Oral Tablet, Film Coated
Application #: NDA022568
Rev. Date: 


NDC Package Codes:

  • 75929-087-03: 30 TABLET, FILM COATED IN 1 BOTTLE (75929‑087‑03)

Active Ingredients:

  • Donepezil Hydrochloride

Dosage Strength:

  • 23 mg

Pharmaceutical Classes:

  • Cholinesterase Inhibitor [EPC]
  • Cholinesterase Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 75929-086 Aricept 10 mg Oral Tablet, Film Coated by Pharma Packaging Solutions, LLC Dba Tjoapack LLC
  • 54868-3952 Aricept 5 mg Oral Tablet by Physicians Total Care, Inc.
  • 54868-4245 Aricept 10 mg Oral Tablet by Physicians Total Care, Inc.
  • 55154-2450 Aricept 5 mg Oral Tablet by Cardinal Health
  • 55154-2452 Aricept 10 mg Oral Tablet by Cardinal Health
  • 55289-151 Aricept 10 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
  • 62856-245 Aricept 5 mg Oral Tablet by Eisai Inc.
  • 62856-246 Aricept 10 mg Oral Tablet by Eisai Inc.
  • 62856-247 Aricept 23 mg Oral Tablet by Eisai Inc.
  • 62856-831 Aricept 5 mg Disintegrating Tablet by Eisai Inc.
  • 62856-832 Aricept 10 mg Disintegrating Tablet by Eisai Inc.
  • 63629-3632 Aricept 10 mg Oral Tablet by Bryant Ranch Prepack
  • 69189-0247 Aricept 23 mg Oral Tablet, Film Coated by Avera Mckennan Hospital

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.