aripiprazole

Generic: aripiprazole

Labeler: sciegen pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler sciegen pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 15 mg/1

Manufacturer
ScieGen Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 50228-327
Product ID 50228-327_8fbc9a67-ee90-4b5d-b9be-a037bef430de
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206383
Listing Expiration 2026-12-31
Marketing Start 2016-09-29

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50228327
Hyphenated Format 50228-327

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0350228324106 0350228328302 0350228324304 0350228329309 0350228325301 0350228327107 0350228326100 0350228327305 0350228329101 0350228326308 0350228328104 0350228325103
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 ANDA206383 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (50228-327-10)
  • 30 TABLET in 1 BOTTLE (50228-327-30)
source: ndc

Packages (2)

Ingredients (1)

aripiprazole (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8fbc9a67-ee90-4b5d-b9be-a037bef430de", "openfda": {"nui": ["N0000175430"], "upc": ["0350228324106", "0350228328302", "0350228324304", "0350228329309", "0350228325301", "0350228327107", "0350228326100", "0350228327305", "0350228329101", "0350228326308", "0350228328104", "0350228325103"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["95954ba3-e838-4dd7-aef1-c51ac6aff76b"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["ScieGen Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (50228-327-10)", "package_ndc": "50228-327-10", "marketing_start_date": "20160929"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-327-30)", "package_ndc": "50228-327-30", "marketing_start_date": "20160929"}], "brand_name": "Aripiprazole", "product_id": "50228-327_8fbc9a67-ee90-4b5d-b9be-a037bef430de", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50228-327", "generic_name": "Aripiprazole", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "15 mg/1"}], "application_number": "ANDA206383", "marketing_category": "ANDA", "marketing_start_date": "20160929", "listing_expiration_date": "20261231"}