aripiprazole

Generic: aripiprazole

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 2 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7564
Product ID 50090-7564_eed092cc-c2c1-4bf5-b2a2-6648412018a8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203908
Listing Expiration 2026-12-31
Marketing Start 2015-10-08

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907564
Hyphenated Format 50090-7564

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 ANDA203908 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7564-0)
  • 90 TABLET in 1 BOTTLE (50090-7564-1)
source: ndc

Packages (2)

Ingredients (1)

aripiprazole (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eed092cc-c2c1-4bf5-b2a2-6648412018a8", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["a8edb057-18a3-446d-8af0-672c97933a88"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7564-0)", "package_ndc": "50090-7564-0", "marketing_start_date": "20250528"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7564-1)", "package_ndc": "50090-7564-1", "marketing_start_date": "20250528"}], "brand_name": "Aripiprazole", "product_id": "50090-7564_eed092cc-c2c1-4bf5-b2a2-6648412018a8", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-7564", "generic_name": "Aripiprazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA203908", "marketing_category": "ANDA", "marketing_start_date": "20151008", "listing_expiration_date": "20261231"}