donepezil

Generic: donepezil hydrochloride

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil
Generic Name donepezil hydrochloride
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-738
Product ID 31722-738_2b1d0795-adc8-39e4-e063-6294a90a91cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203034
Listing Expiration 2026-12-31
Marketing Start 2015-02-02

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722738
Hyphenated Format 31722-738

Supplemental Identifiers

RxCUI
997223 997229
UPC
0331722737302 0331722738309
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 (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 TABLET in 1 BOTTLE (31722-738-01)
  • 500 TABLET in 1 BOTTLE (31722-738-05)
  • 30 TABLET in 1 BOTTLE (31722-738-30)
  • 100 TABLET in 1 BLISTER PACK (31722-738-31)
  • 90 TABLET in 1 BOTTLE (31722-738-90)
source: ndc

Packages (5)

31722-738-01 100 TABLET in 1 BOTTLE (31722-738-01) 31722-738-05 500 TABLET in 1 BOTTLE (31722-738-05) 31722-738-30 30 TABLET in 1 BOTTLE (31722-738-30) 31722-738-31 100 TABLET in 1 BLISTER PACK (31722-738-31) 31722-738-90 90 TABLET in 1 BOTTLE (31722-738-90)

Ingredients (1)

donepezil hydrochloride (10 mg/1)

Linked Drug Pages (1)

Donepezil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b1d0795-adc8-39e4-e063-6294a90a91cb", "openfda": {"upc": ["0331722737302", "0331722738309"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["11ac01f4-d26e-47b2-9660-d514ab097fdb"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-738-01)", "package_ndc": "31722-738-01", "marketing_start_date": "20150202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-738-05)", "package_ndc": "31722-738-05", "marketing_start_date": "20150202"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (31722-738-30)", "package_ndc": "31722-738-30", "marketing_start_date": "20150202"}, {"sample": false, "description": "100 TABLET in 1 BLISTER PACK (31722-738-31)", "package_ndc": "31722-738-31", "marketing_start_date": "20150202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (31722-738-90)", "package_ndc": "31722-738-90", "marketing_start_date": "20150202"}], "brand_name": "Donepezil", "product_id": "31722-738_2b1d0795-adc8-39e4-e063-6294a90a91cb", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "31722-738", "generic_name": "Donepezil hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "20150202", "listing_expiration_date": "20261231"}