aripiprazole

Generic: aripiprazole

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 2 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-466
Product ID 72189-466_2c4def88-252d-7c8b-e063-6294a90aeb94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207105
Listing Expiration 2026-12-31
Marketing Start 2023-05-03

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189466
Hyphenated Format 72189-466

Supplemental Identifiers

RxCUI
602964
UNII
82VFR53I78
NUI
N0000175430

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 aripiprazole (source: ndc)
Generic Name aripiprazole (source: ndc)
Application Number ANDA207105 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-466-30)
source: ndc

Packages (1)

72189-466-30 30 TABLET in 1 BOTTLE (72189-466-30)

Ingredients (1)

aripiprazole (2 mg/1)

Linked Drug Pages (1)

Aripiprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4def88-252d-7c8b-e063-6294a90aeb94", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["facdb9a9-612f-e59a-e053-6394a90a1fa7"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-466-30)", "package_ndc": "72189-466-30", "marketing_start_date": "20230503"}], "brand_name": "Aripiprazole", "product_id": "72189-466_2c4def88-252d-7c8b-e063-6294a90aeb94", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-466", "generic_name": "Aripiprazole", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20230503", "listing_expiration_date": "20261231"}