aripiprazole

Generic: aripiprazole

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-235
Product ID 82804-235_2c2b0172-b186-4be4-a002-4a26adf120c6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201519
Listing Expiration 2026-12-31
Marketing Start 2015-04-28

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804235
Hyphenated Format 82804-235

Supplemental Identifiers

RxCUI
402131
UPC
0382804235902
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 ANDA201519 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (82804-235-90)
source: ndc

Packages (1)

82804-235-90 90 TABLET in 1 BOTTLE (82804-235-90)

Ingredients (1)

aripiprazole (5 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": "2c2b0172-b186-4be4-a002-4a26adf120c6", "openfda": {"nui": ["N0000175430"], "upc": ["0382804235902"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["2c2b0172-b186-4be4-a002-4a26adf120c6"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-235-90)", "package_ndc": "82804-235-90", "marketing_start_date": "20250819"}], "brand_name": "aripiprazole", "product_id": "82804-235_2c2b0172-b186-4be4-a002-4a26adf120c6", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82804-235", "generic_name": "aripiprazole", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}