aripiprazole
Generic: aripiprazole
Labeler: quagen pharmaceuticals llcDrug Facts
Product Profile
Brand Name
aripiprazole
Generic Name
aripiprazole
Labeler
quagen pharmaceuticals llc
Dosage Form
SOLUTION
Routes
Active Ingredients
aripiprazole 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70752-114
Product ID
70752-114_f53a4fb5-9152-4ccc-82fb-f45ea242c03d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215582
Listing Expiration
2026-12-31
Marketing Start
2025-12-15
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70752114
Hyphenated Format
70752-114
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
ANDA215582 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (70752-114-07) / 150 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f53a4fb5-9152-4ccc-82fb-f45ea242c03d", "openfda": {"nui": ["N0000175430"], "upc": ["0370752114073"], "unii": ["82VFR53I78"], "rxcui": ["485496"], "spl_set_id": ["b12f1ff2-c0b5-47e7-8075-bf2ce79fdaf8"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70752-114-07) / 150 mL in 1 BOTTLE", "package_ndc": "70752-114-07", "marketing_start_date": "20251215"}], "brand_name": "ARIPIPRAZOLE", "product_id": "70752-114_f53a4fb5-9152-4ccc-82fb-f45ea242c03d", "dosage_form": "SOLUTION", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70752-114", "generic_name": "ARIPIPRAZOLE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARIPIPRAZOLE", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "1 mg/mL"}], "application_number": "ANDA215582", "marketing_category": "ANDA", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}