aripiprazole

Generic: aripiprazole

Labeler: xlcare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler xlcare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 20 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72865-157
Product ID 72865-157_f26f3784-b822-9efd-e053-2a95a90ab6ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205064
Listing Expiration 2026-12-31
Marketing Start 2020-11-20

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865157
Hyphenated Format 72865-157

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0372865155059 0372865153055 0372865154052
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 ANDA205064 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (72865-157-05)
  • 30 TABLET in 1 BOTTLE (72865-157-30)
source: ndc

Packages (2)

72865-157-05 500 TABLET in 1 BOTTLE (72865-157-05) 72865-157-30 30 TABLET in 1 BOTTLE (72865-157-30)

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": "f26f3784-b822-9efd-e053-2a95a90ab6ee", "openfda": {"nui": ["N0000175430"], "upc": ["0372865155059", "0372865153055", "0372865154052"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["b284b294-40a0-4ccd-b7b7-b61267cd4e76"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-157-05)", "package_ndc": "72865-157-05", "marketing_start_date": "20201120"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72865-157-30)", "package_ndc": "72865-157-30", "marketing_start_date": "20201120"}], "brand_name": "Aripiprazole", "product_id": "72865-157_f26f3784-b822-9efd-e053-2a95a90ab6ee", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72865-157", "generic_name": "Aripiprazole", "labeler_name": "XLCare Pharmaceuticals, Inc.", "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": "20201120", "listing_expiration_date": "20261231"}