aripiprazole

Generic: aripiprazole

Labeler: ajanta pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler ajanta pharma usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 10 mg/1

Manufacturer
Ajanta Pharma USA Inc.

Identifiers & Regulatory

Product NDC 27241-053
Product ID 27241-053_2a724a23-cf45-4d22-90f5-ebe68f9b7ab9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206174
Listing Expiration 2026-12-31
Marketing Start 2017-05-30

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27241053
Hyphenated Format 27241-053

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0327241051036 0327241055034 0327241053030 0327241056031 0327241054037 0327241052033
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 ANDA206174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (27241-053-03)
  • 500 TABLET in 1 BOTTLE (27241-053-08)
source: ndc

Packages (2)

Ingredients (1)

aripiprazole (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a724a23-cf45-4d22-90f5-ebe68f9b7ab9", "openfda": {"nui": ["N0000175430"], "upc": ["0327241051036", "0327241055034", "0327241053030", "0327241056031", "0327241054037", "0327241052033"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["d0f910b5-adef-4a93-9369-70f1ed541503"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Ajanta Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (27241-053-03)", "package_ndc": "27241-053-03", "marketing_start_date": "20170530"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (27241-053-08)", "package_ndc": "27241-053-08", "marketing_start_date": "20170530"}], "brand_name": "Aripiprazole", "product_id": "27241-053_2a724a23-cf45-4d22-90f5-ebe68f9b7ab9", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "27241-053", "generic_name": "Aripiprazole", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA206174", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}