donepezil
Generic: donepezil hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
donepezil
Generic Name
donepezil hydrochloride
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
donepezil hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-292
Product ID
60687-292_3f922a89-21fe-d605-e063-6294a90a8b8d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203034
Listing Expiration
2026-12-31
Marketing Start
2017-05-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687292
Hyphenated Format
60687-292
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-292-01) / 1 TABLET in 1 BLISTER PACK (60687-292-11)
Packages (1)
Ingredients (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 (60687-292-01) / 1 TABLET in 1 BLISTER PACK (60687-292-11)", "package_ndc": "60687-292-01", "marketing_start_date": "20170517"}], "brand_name": "Donepezil", "product_id": "60687-292_3f922a89-21fe-d605-e063-6294a90a8b8d", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "60687-292", "generic_name": "Donepezil hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203034", "marketing_category": "ANDA", "marketing_start_date": "20170517", "listing_expiration_date": "20261231"}