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 2 mg/1

Manufacturer
ScieGen Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 50228-475
Product ID 50228-475_f52587a6-f60d-515d-e053-2995a90aadb8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206383
Listing Expiration 2026-12-31
Marketing Start 2020-02-25

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50228475
Hyphenated Format 50228-475

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0350228480307 0350228475303 0350228480109 0350228479103 0350228478106 0350228477307 0350228475105 0350228476102 0350228477109 0350228479301 0350228476300 0350228478304
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
  • 2 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (50228-475-10)
  • 30 TABLET in 1 BOTTLE (50228-475-30)
source: ndc

Packages (2)

50228-475-10 1000 TABLET in 1 BOTTLE (50228-475-10) 50228-475-30 30 TABLET in 1 BOTTLE (50228-475-30)

Ingredients (1)

aripiprazole (2 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": "f52587a6-f60d-515d-e053-2995a90aadb8", "openfda": {"nui": ["N0000175430"], "upc": ["0350228480307", "0350228475303", "0350228480109", "0350228479103", "0350228478106", "0350228477307", "0350228475105", "0350228476102", "0350228477109", "0350228479301", "0350228476300", "0350228478304"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["a7d9d5d1-25ba-4f4e-a990-398c0bf09c7e"], "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 (50228-475-10)", "package_ndc": "50228-475-10", "marketing_start_date": "20200225"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50228-475-30)", "package_ndc": "50228-475-30", "marketing_start_date": "20200225"}], "brand_name": "Aripiprazole", "product_id": "50228-475_f52587a6-f60d-515d-e053-2995a90aadb8", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50228-475", "generic_name": "Aripiprazole", "labeler_name": "ScieGen Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA206383", "marketing_category": "ANDA", "marketing_start_date": "20200225", "listing_expiration_date": "20261231"}