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 2 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3725
Product ID 68071-3725_27877179-645e-dcc2-e063-6394a90aa66c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207105
Listing Expiration 2026-12-31
Marketing Start 2019-02-27

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713725
Hyphenated Format 68071-3725

Supplemental Identifiers

RxCUI
602964
UPC
0368071372533
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 ANDA207105 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3725-3)
source: ndc

Packages (1)

68071-3725-3 30 TABLET in 1 BOTTLE (68071-3725-3)

Ingredients (1)

aripiprazole (2 mg/1)

Linked Drug Pages (1)

Aripiprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "27877179-645e-dcc2-e063-6394a90aa66c", "openfda": {"nui": ["N0000175430"], "upc": ["0368071372533"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["27874fe2-3fd6-002d-e063-6294a90a4cd7"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3725-3)", "package_ndc": "68071-3725-3", "marketing_start_date": "20241122"}], "brand_name": "Aripiprazole", "product_id": "68071-3725_27877179-645e-dcc2-e063-6394a90aa66c", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68071-3725", "generic_name": "Aripiprazole", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20190227", "listing_expiration_date": "20261231"}