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 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7125
Product ID 50090-7125_fc6e3258-1414-499b-853e-8d4809d51b43
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205064
Listing Expiration 2026-12-31
Marketing Start 2020-10-01

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907125
Hyphenated Format 50090-7125

Supplemental Identifiers

RxCUI
349553
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 ANDA205064 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7125-0)
source: ndc

Packages (1)

50090-7125-0 30 TABLET in 1 BOTTLE (50090-7125-0)

Ingredients (1)

aripiprazole (20 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": "fc6e3258-1414-499b-853e-8d4809d51b43", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["89c2cddc-2ae3-4505-adf9-018542c713bf"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7125-0)", "package_ndc": "50090-7125-0", "marketing_start_date": "20240409"}], "brand_name": "Aripiprazole", "product_id": "50090-7125_fc6e3258-1414-499b-853e-8d4809d51b43", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-7125", "generic_name": "Aripiprazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}