aripiprazole
Generic: aripiprazole
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
aripiprazole
Generic Name
aripiprazole
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
aripiprazole 15 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8502
Product ID
68788-8502_b3046f28-ea00-4035-9a18-02f3d37e43b5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202101
Listing Expiration
2027-12-31
Marketing Start
2023-08-09
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888502
Hyphenated Format
68788-8502
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA202101 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 mg/1
Packaging
- 100 TABLET in 1 CARTON (68788-8502-1)
- 20 TABLET in 1 BOTTLE (68788-8502-2)
- 30 TABLET in 1 BOTTLE (68788-8502-3)
- 60 TABLET in 1 BOTTLE (68788-8502-6)
- 90 TABLET in 1 BOTTLE (68788-8502-9)
Packages (5)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b3046f28-ea00-4035-9a18-02f3d37e43b5", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349490"], "spl_set_id": ["02a4af27-c83c-4166-950c-7a1cb12d198d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 CARTON (68788-8502-1)", "package_ndc": "68788-8502-1", "marketing_start_date": "20230809"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-8502-2)", "package_ndc": "68788-8502-2", "marketing_start_date": "20230809"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8502-3)", "package_ndc": "68788-8502-3", "marketing_start_date": "20230809"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8502-6)", "package_ndc": "68788-8502-6", "marketing_start_date": "20230809"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8502-9)", "package_ndc": "68788-8502-9", "marketing_start_date": "20230809"}], "brand_name": "Aripiprazole", "product_id": "68788-8502_b3046f28-ea00-4035-9a18-02f3d37e43b5", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68788-8502", "generic_name": "Aripiprazole", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "15 mg/1"}], "application_number": "ANDA202101", "marketing_category": "ANDA", "marketing_start_date": "20230809", "listing_expiration_date": "20271231"}