aripiprazole
Generic: aripiprazole
Labeler: st. mary's medical park pharmacyDrug Facts
Product Profile
Brand Name
aripiprazole
Generic Name
aripiprazole
Labeler
st. mary's medical park pharmacy
Dosage Form
TABLET
Routes
Active Ingredients
aripiprazole 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60760-691
Product ID
60760-691_35a85fd5-5a85-78c7-e063-6294a90ab203
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)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60760691
Hyphenated Format
60760-691
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
ANDA201519 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (60760-691-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35a85fd5-5a85-78c7-e063-6294a90ab203", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["35a86989-862e-b0bb-e063-6394a90a7ec1"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-691-30)", "package_ndc": "60760-691-30", "marketing_start_date": "20250513"}], "brand_name": "aripiprazole", "product_id": "60760-691_35a85fd5-5a85-78c7-e063-6294a90ab203", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "60760-691", "generic_name": "aripiprazole", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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"}