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 50090-6063
Product ID 50090-6063_6cd1204f-119f-4913-8065-f458f2c4598f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206251
Listing Expiration 2026-12-31
Marketing Start 2017-02-15

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906063
Hyphenated Format 50090-6063

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 ANDA206251 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6063-0)
source: ndc

Packages (1)

Ingredients (1)

aripiprazole (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6cd1204f-119f-4913-8065-f458f2c4598f", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["aaf7dc7e-04f3-442b-86d7-5f54d17d102c"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6063-0)", "package_ndc": "50090-6063-0", "marketing_start_date": "20220907"}], "brand_name": "ARIPIPRAZOLE", "product_id": "50090-6063_6cd1204f-119f-4913-8065-f458f2c4598f", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-6063", "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": "ANDA206251", "marketing_category": "ANDA", "marketing_start_date": "20170215", "listing_expiration_date": "20261231"}