aripiprazole
Generic: aripiprazole
Labeler: ajanta pharma usa inc.Drug Facts
Product Profile
Brand Name
aripiprazole
Generic Name
aripiprazole
Labeler
ajanta pharma usa inc.
Dosage Form
TABLET
Routes
Active Ingredients
aripiprazole 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
27241-056
Product ID
27241-056_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)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
27241056
Hyphenated Format
27241-056
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (27241-056-03)
- 500 TABLET in 1 BOTTLE (27241-056-08)
Packages (2)
Ingredients (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 (27241-056-03)", "package_ndc": "27241-056-03", "marketing_start_date": "20170530"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (27241-056-08)", "package_ndc": "27241-056-08", "marketing_start_date": "20170530"}], "brand_name": "Aripiprazole", "product_id": "27241-056_2a724a23-cf45-4d22-90f5-ebe68f9b7ab9", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "27241-056", "generic_name": "Aripiprazole", "labeler_name": "Ajanta Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA206174", "marketing_category": "ANDA", "marketing_start_date": "20170530", "listing_expiration_date": "20261231"}