aripiprazole

Generic: aripiprazole

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 5 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3848
Product ID 68071-3848_3cf72865-97f2-2fea-e063-6394a90ab9cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205064
Listing Expiration 2026-12-31
Marketing Start 2015-04-28

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713848
Hyphenated Format 68071-3848

Supplemental Identifiers

RxCUI
402131
UPC
0368071384833
UNII
82VFR53I78
NUI
N0000175430

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 ANDA205064 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3848-3)
source: ndc

Packages (1)

Ingredients (1)

aripiprazole (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3cf72865-97f2-2fea-e063-6394a90ab9cb", "openfda": {"nui": ["N0000175430"], "upc": ["0368071384833"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["3cf72cc6-ae43-bfd5-e063-6294a90a18b0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3848-3)", "package_ndc": "68071-3848-3", "marketing_start_date": "20250822"}], "brand_name": "Aripiprazole", "product_id": "68071-3848_3cf72865-97f2-2fea-e063-6394a90ab9cb", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3848", "generic_name": "Aripiprazole", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}