donepezil hydrochloride
Generic: donepezil hydrochloride
Labeler: hisun pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
donepezil hydrochloride
Generic Name
donepezil hydrochloride
Labeler
hisun pharmaceuticals usa, inc.
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
donepezil hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42658-120
Product ID
42658-120_2c703e82-e970-a97e-e063-6294a90a1639
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205269
Listing Expiration
2026-12-31
Marketing Start
2025-01-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42658120
Hyphenated Format
42658-120
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 hydrochloride (source: ndc)
Generic Name
donepezil hydrochloride (source: ndc)
Application Number
ANDA205269 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-01)
- 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-04)
- 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-08)
- 3 BLISTER PACK in 1 CARTON (42658-120-51) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Packages (4)
42658-120-01
30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-01)
42658-120-04
90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-04)
42658-120-08
1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-08)
42658-120-51
3 BLISTER PACK in 1 CARTON (42658-120-51) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c703e82-e970-a97e-e063-6294a90a1639", "openfda": {"upc": ["0342658120083", "0342658119087", "0342658119513", "0342658120014", "0342658119049", "0342658119018", "0342658120519", "0342658120045"], "unii": ["3O2T2PJ89D"], "rxcui": ["997220", "997226"], "spl_set_id": ["8d682a51-31d0-43e6-9fab-6eb5219f5a41"], "manufacturer_name": ["Hisun Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-01)", "package_ndc": "42658-120-01", "marketing_start_date": "20250101"}, {"sample": false, "description": "90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-04)", "package_ndc": "42658-120-04", "marketing_start_date": "20250101"}, {"sample": false, "description": "1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-08)", "package_ndc": "42658-120-08", "marketing_start_date": "20250101"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (42658-120-51) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "42658-120-51", "marketing_start_date": "20250101"}], "brand_name": "Donepezil Hydrochloride", "product_id": "42658-120_2c703e82-e970-a97e-e063-6294a90a1639", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "42658-120", "generic_name": "donepezil hydrochloride", "labeler_name": "Hisun Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205269", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}