aripiprazole

Generic: aripiprazole

Labeler: solco healthcare u.s., llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler solco healthcare u.s., llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 2 mg/1

Manufacturer
Solco Healthcare U.S., LLC

Identifiers & Regulatory

Product NDC 43547-884
Product ID 43547-884_abb8ad7e-7998-4485-a09f-a2892190f4ad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205363
Listing Expiration 2026-12-31
Marketing Start 2017-12-04

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43547884
Hyphenated Format 43547-884

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0343547889036 0343547884031 0343547885038 0343547887032 0343547886035 0343547888039
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 ANDA205363 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (43547-884-03)
  • 500 TABLET in 1 BOTTLE (43547-884-50)
source: ndc

Packages (2)

Ingredients (1)

aripiprazole (2 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "abb8ad7e-7998-4485-a09f-a2892190f4ad", "openfda": {"nui": ["N0000175430"], "upc": ["0343547889036", "0343547884031", "0343547885038", "0343547887032", "0343547886035", "0343547888039"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["abb8ad7e-7998-4485-a09f-a2892190f4ad"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Solco Healthcare U.S., LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (43547-884-03)", "package_ndc": "43547-884-03", "marketing_start_date": "20171204"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43547-884-50)", "package_ndc": "43547-884-50", "marketing_start_date": "20171204"}], "brand_name": "ARIPIPRAZOLE", "product_id": "43547-884_abb8ad7e-7998-4485-a09f-a2892190f4ad", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43547-884", "generic_name": "aripiprazole", "labeler_name": "Solco Healthcare U.S., LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARIPIPRAZOLE", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA205363", "marketing_category": "ANDA", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}