donepezil

Generic: donepezil hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil
Generic Name donepezil hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2627
Product ID 50090-2627_1eda014d-ec3c-4940-a6a2-3dfe24b07712
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203034
Listing Expiration 2027-12-31
Marketing Start 2015-02-02

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902627
Hyphenated Format 50090-2627

Supplemental Identifiers

RxCUI
997223 997229
UNII
3O2T2PJ89D

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name donepezil (source: ndc)
Generic Name donepezil hydrochloride (source: ndc)
Application Number ANDA203034 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-2627-0)
source: ndc

Packages (1)

50090-2627-0 90 TABLET in 1 BOTTLE (50090-2627-0)

Ingredients (1)

donepezil hydrochloride (10 mg/1)

Linked Drug Pages (1)

Donepezil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1eda014d-ec3c-4940-a6a2-3dfe24b07712", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["84d8ca68-26f3-4dd5-9dd4-6a7525a30db1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-2627-0)", "package_ndc": "50090-2627-0", "marketing_start_date": "20161117"}], "brand_name": "Donepezil", "product_id": "50090-2627_1eda014d-ec3c-4940-a6a2-3dfe24b07712", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "50090-2627", "generic_name": "Donepezil hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203034", "marketing_category": "ANDA", "marketing_start_date": "20150202", "listing_expiration_date": "20271231"}