aripiprazole

Generic: aripiprazole

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0412
Product ID 71335-0412_08e95ea0-2263-44d4-9b1c-49e8426bafe0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201519
Listing Expiration 2026-12-31
Marketing Start 2015-04-28

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350412
Hyphenated Format 71335-0412

Supplemental Identifiers

RxCUI
349553
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 ANDA201519 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0412-1)
  • 28 TABLET in 1 BOTTLE (71335-0412-2)
  • 90 TABLET in 1 BOTTLE (71335-0412-3)
source: ndc

Packages (3)

71335-0412-1 30 TABLET in 1 BOTTLE (71335-0412-1) 71335-0412-2 28 TABLET in 1 BOTTLE (71335-0412-2) 71335-0412-3 90 TABLET in 1 BOTTLE (71335-0412-3)

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": "08e95ea0-2263-44d4-9b1c-49e8426bafe0", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["e7b6a156-8001-441c-bfd3-bf8987a339e8"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0412-1)", "package_ndc": "71335-0412-1", "marketing_start_date": "20180315"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0412-2)", "package_ndc": "71335-0412-2", "marketing_start_date": "20241030"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0412-3)", "package_ndc": "71335-0412-3", "marketing_start_date": "20190611"}], "brand_name": "aripiprazole", "product_id": "71335-0412_08e95ea0-2263-44d4-9b1c-49e8426bafe0", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-0412", "generic_name": "aripiprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}