donepezil hydrochloride

Generic: donepezil hydrochloride

Labeler: torrent pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil hydrochloride
Generic Name donepezil hydrochloride
Labeler torrent pharmaceuticals limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-103
Product ID 13668-103_bc153659-2091-4682-a63b-8735e1146bac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090686
Listing Expiration 2027-12-31
Marketing Start 2011-05-31

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13668103
Hyphenated Format 13668-103

Supplemental Identifiers

RxCUI
997223 997229
UPC
0313668102307 0313668103304
UNII
3O2T2PJ89D

Packaging Origin

Original Packager
true

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 ANDA090686 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (13668-103-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (13668-103-10)
  • 2650 TABLET, FILM COATED in 1 BOTTLE (13668-103-26)
  • 30 TABLET, FILM COATED in 1 BOTTLE (13668-103-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (13668-103-90)
source: ndc

Packages (5)

13668-103-05 500 TABLET, FILM COATED in 1 BOTTLE (13668-103-05) 13668-103-10 1000 TABLET, FILM COATED in 1 BOTTLE (13668-103-10) 13668-103-26 2650 TABLET, FILM COATED in 1 BOTTLE (13668-103-26) 13668-103-30 30 TABLET, FILM COATED in 1 BOTTLE (13668-103-30) 13668-103-90 90 TABLET, FILM COATED in 1 BOTTLE (13668-103-90)

Ingredients (1)

donepezil hydrochloride (10 mg/1)

Linked Drug Pages (1)

Donepezil Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "bc153659-2091-4682-a63b-8735e1146bac", "openfda": {"upc": ["0313668102307", "0313668103304"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["76bf638e-dbde-418e-8977-1caf009990bc"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13668-103-05)", "package_ndc": "13668-103-05", "marketing_start_date": "20110531"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (13668-103-10)", "package_ndc": "13668-103-10", "marketing_start_date": "20110531"}, {"sample": false, "description": "2650 TABLET, FILM COATED in 1 BOTTLE (13668-103-26)", "package_ndc": "13668-103-26", "marketing_start_date": "20110531"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-103-30)", "package_ndc": "13668-103-30", "marketing_start_date": "20110531"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (13668-103-90)", "package_ndc": "13668-103-90", "marketing_start_date": "20110531"}], "brand_name": "Donepezil Hydrochloride", "product_id": "13668-103_bc153659-2091-4682-a63b-8735e1146bac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "13668-103", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090686", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20271231"}