donepezil hydrochloride
Generic: donepezil hydrochloride
Labeler: dr. reddys laboratories limitedDrug Facts
Product Profile
Brand Name
donepezil hydrochloride
Generic Name
donepezil hydrochloride
Labeler
dr. reddys laboratories limited
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
donepezil hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55111-357
Product ID
55111-357_d6af4584-b379-0cea-78b6-a493f88708c8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201001
Listing Expiration
2026-12-31
Marketing Start
2011-05-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55111357
Hyphenated Format
55111-357
Supplemental Identifiers
RxCUI
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
ANDA201001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 500 TABLET, FILM COATED in 1 BOTTLE (55111-357-05)
- 1000 TABLET, FILM COATED in 1 BOTTLE (55111-357-10)
- 30 TABLET, FILM COATED in 1 BOTTLE (55111-357-30)
- 10 BLISTER PACK in 1 CARTON (55111-357-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-357-79)
- 90 TABLET, FILM COATED in 1 BOTTLE (55111-357-90)
Packages (5)
55111-357-05
500 TABLET, FILM COATED in 1 BOTTLE (55111-357-05)
55111-357-10
1000 TABLET, FILM COATED in 1 BOTTLE (55111-357-10)
55111-357-30
30 TABLET, FILM COATED in 1 BOTTLE (55111-357-30)
55111-357-78
10 BLISTER PACK in 1 CARTON (55111-357-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-357-79)
55111-357-90
90 TABLET, FILM COATED in 1 BOTTLE (55111-357-90)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d6af4584-b379-0cea-78b6-a493f88708c8", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["4c9889fd-2cb3-02da-f034-46120acc38c3"], "manufacturer_name": ["Dr. Reddys Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (55111-357-05)", "package_ndc": "55111-357-05", "marketing_start_date": "20110531"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (55111-357-10)", "package_ndc": "55111-357-10", "marketing_start_date": "20110531"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-357-30)", "package_ndc": "55111-357-30", "marketing_start_date": "20110531"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-357-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-357-79)", "package_ndc": "55111-357-78", "marketing_start_date": "20110531"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (55111-357-90)", "package_ndc": "55111-357-90", "marketing_start_date": "20110531"}], "brand_name": "Donepezil hydrochloride", "product_id": "55111-357_d6af4584-b379-0cea-78b6-a493f88708c8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "55111-357", "generic_name": "Donepezil hydrochloride", "labeler_name": "Dr. Reddys Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201001", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20261231"}