donepezil

Generic: donepezil hydrochloride

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil
Generic Name donepezil hydrochloride
Labeler american health packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-303
Product ID 60687-303_3f922a89-21fe-d605-e063-6294a90a8b8d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203034
Listing Expiration 2026-12-31
Marketing Start 2017-03-21

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687303
Hyphenated Format 60687-303

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
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-303-01) / 1 TABLET in 1 BLISTER PACK (60687-303-11)
source: ndc

Packages (1)

Ingredients (1)

donepezil hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f922a89-21fe-d605-e063-6294a90a8b8d", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["12ae85f0-023c-49ca-8c4a-0a6a7585290e"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-303-01)  / 1 TABLET in 1 BLISTER PACK (60687-303-11)", "package_ndc": "60687-303-01", "marketing_start_date": "20170321"}], "brand_name": "Donepezil", "product_id": "60687-303_3f922a89-21fe-d605-e063-6294a90a8b8d", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "60687-303", "generic_name": "Donepezil hydrochloride", "labeler_name": "American Health Packaging", "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": "20170321", "listing_expiration_date": "20261231"}