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 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4936
Product ID 50090-4936_4e29d321-b967-427a-ba5b-a7959fcb08e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207105
Listing Expiration 2027-12-31
Marketing Start 2019-02-27

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904936
Hyphenated Format 50090-4936

Supplemental Identifiers

RxCUI
349545
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 ANDA207105 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-4936-0)
  • 30 TABLET in 1 BOTTLE (50090-4936-1)
source: ndc

Packages (2)

Ingredients (1)

aripiprazole (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4e29d321-b967-427a-ba5b-a7959fcb08e8", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349545"], "spl_set_id": ["554db933-aa80-4685-bcd5-58c84571c19c"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4936-0)", "package_ndc": "50090-4936-0", "marketing_start_date": "20200227"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4936-1)", "package_ndc": "50090-4936-1", "marketing_start_date": "20200227"}], "brand_name": "Aripiprazole", "product_id": "50090-4936_4e29d321-b967-427a-ba5b-a7959fcb08e8", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-4936", "generic_name": "Aripiprazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20190227", "listing_expiration_date": "20271231"}