Package 82009-089-05
Brand: aripiprazole
Generic: aripiprazolePackage Facts
Identity
Package NDC
82009-089-05
Digits Only
8200908905
Product NDC
82009-089
Description
500 TABLET in 1 BOTTLE (82009-089-05)
Marketing
Marketing Status
Brand
aripiprazole
Generic
aripiprazole
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5c525d81-2a40-4c63-a28c-94865bf0c493", "openfda": {"nui": ["N0000175430"], "upc": ["0382009088051", "0382009090054", "0382009091051", "0382009089058"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "402131", "602964"], "spl_set_id": ["0e0d42ad-f4c6-4e30-adc2-ab1d122428ec"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (82009-089-05)", "package_ndc": "82009-089-05", "marketing_start_date": "20230719"}], "brand_name": "Aripiprazole", "product_id": "82009-089_5c525d81-2a40-4c63-a28c-94865bf0c493", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82009-089", "generic_name": "Aripiprazole", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA206174", "marketing_category": "ANDA", "marketing_start_date": "20230719", "listing_expiration_date": "20261231"}