aripiprazole

Generic: aripiprazole

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler aurobindo pharma limited
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

aripiprazole 1 mg/mL

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-110
Product ID 59651-110_335e176d-01fe-4b63-9e9f-1bdf95c3ae70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210479
Listing Expiration 2026-12-31
Marketing Start 2019-01-29

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651110
Hyphenated Format 59651-110

Supplemental Identifiers

RxCUI
485496
UNII
82VFR53I78
NUI
N0000175430

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 aripiprazole (source: ndc)
Generic Name aripiprazole (source: ndc)
Application Number ANDA210479 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (59651-110-55) / 150 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

aripiprazole (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "335e176d-01fe-4b63-9e9f-1bdf95c3ae70", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["485496"], "spl_set_id": ["fcabd777-dcb7-452c-821c-575a5991c90a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (59651-110-55)  / 150 mL in 1 BOTTLE", "package_ndc": "59651-110-55", "marketing_start_date": "20190129"}], "brand_name": "Aripiprazole", "product_id": "59651-110_335e176d-01fe-4b63-9e9f-1bdf95c3ae70", "dosage_form": "SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "59651-110", "generic_name": "Aripiprazole", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "1 mg/mL"}], "application_number": "ANDA210479", "marketing_category": "ANDA", "marketing_start_date": "20190129", "listing_expiration_date": "20261231"}