donepezil hydrochloride

Generic: donepezil hydrochloride

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name donepezil hydrochloride
Generic Name donepezil hydrochloride
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

donepezil hydrochloride 10 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-251
Product ID 29300-251_88d3f867-45f4-42fb-93f8-235c2f594760
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204831
Listing Expiration 2026-12-31
Marketing Start 2016-11-10

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 29300251
Hyphenated Format 29300-251

Supplemental Identifiers

RxCUI
997220 997223 997226 997229
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 ANDA204831 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (29300-251-87) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (29300-251-11)
source: ndc

Packages (1)

29300-251-87 3 BLISTER PACK in 1 CARTON (29300-251-87) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (29300-251-11)

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": "88d3f867-45f4-42fb-93f8-235c2f594760", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997220", "997223", "997226", "997229"], "spl_set_id": ["1a8906ce-96dc-4bc8-81c1-5db67a187aac"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (29300-251-87)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (29300-251-11)", "package_ndc": "29300-251-87", "marketing_start_date": "20180228"}], "brand_name": "donepezil hydrochloride", "product_id": "29300-251_88d3f867-45f4-42fb-93f8-235c2f594760", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "29300-251", "generic_name": "donepezil hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204831", "marketing_category": "ANDA", "marketing_start_date": "20161110", "listing_expiration_date": "20261231"}