aripiprazole

Generic: aripiprazole

Labeler: quagen pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler quagen pharmaceuticals llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

aripiprazole 1 mg/mL

Manufacturer
QUAGEN PHARMACEUTICALS LLC

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)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70752114
Hyphenated Format 70752-114

Supplemental Identifiers

RxCUI
485496
UPC
0370752114073
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 ANDA215582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (70752-114-07) / 150 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

aripiprazole (1 mg/mL)

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"}