aripiprazole

Generic: aripiprazole

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-392
Product ID 71205-392_ced62de0-d150-4ff8-a1ab-38ef67c8f061
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203908
Listing Expiration 2026-12-31
Marketing Start 2015-10-08

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205392
Hyphenated Format 71205-392

Supplemental Identifiers

RxCUI
402131
UPC
0371205392307
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 ANDA203908 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-392-30)
  • 60 TABLET in 1 BOTTLE (71205-392-60)
  • 90 TABLET in 1 BOTTLE (71205-392-90)
source: ndc

Packages (3)

71205-392-30 30 TABLET in 1 BOTTLE (71205-392-30) 71205-392-60 60 TABLET in 1 BOTTLE (71205-392-60) 71205-392-90 90 TABLET in 1 BOTTLE (71205-392-90)

Ingredients (1)

aripiprazole (5 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": "ced62de0-d150-4ff8-a1ab-38ef67c8f061", "openfda": {"nui": ["N0000175430"], "upc": ["0371205392307"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["11202c0a-7401-41c9-b1e7-d93739fcd36f"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-392-30)", "package_ndc": "71205-392-30", "marketing_start_date": "20200130"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-392-60)", "package_ndc": "71205-392-60", "marketing_start_date": "20200130"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-392-90)", "package_ndc": "71205-392-90", "marketing_start_date": "20200130"}], "brand_name": "Aripiprazole", "product_id": "71205-392_ced62de0-d150-4ff8-a1ab-38ef67c8f061", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71205-392", "generic_name": "Aripiprazole", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA203908", "marketing_category": "ANDA", "marketing_start_date": "20151008", "listing_expiration_date": "20261231"}