Package 42806-338-01

Brand: molindone hydrochloride

Generic: molindone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-338-01
Digits Only 4280633801
Product NDC 42806-338
Description

100 TABLET in 1 BOTTLE (42806-338-01)

Marketing

Marketing Status
Marketed Since 2018-10-17
Brand molindone hydrochloride
Generic molindone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d7c8ea49-c06c-441d-820e-def3920f7c1e", "openfda": {"upc": ["0342806337011"], "unii": ["1DWS68PNE6"], "rxcui": ["1298816", "1298906", "1298910"], "spl_set_id": ["1275e92f-9573-4d0c-8e77-1c9ac47696d2"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-338-01)", "package_ndc": "42806-338-01", "marketing_start_date": "20181017"}], "brand_name": "Molindone Hydrochloride", "product_id": "42806-338_d7c8ea49-c06c-441d-820e-def3920f7c1e", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "42806-338", "generic_name": "Molindone Hydrochloride", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Molindone Hydrochloride", "active_ingredients": [{"name": "MOLINDONE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA090453", "marketing_category": "ANDA", "marketing_start_date": "20181017", "listing_expiration_date": "20261231"}