Package 42806-832-01

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-832-01
Digits Only 4280683201
Product NDC 42806-832
Description

100 CAPSULE in 1 BOTTLE (42806-832-01)

Marketing

Marketing Status
Marketed Since 2025-03-13
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "160f52d2-2e08-4969-80c3-c653767652f0", "openfda": {"upc": ["0342806832011"], "unii": ["TK65WKS8HL"], "rxcui": ["2708991", "2708993", "2708994"], "spl_set_id": ["160f52d2-2e08-4969-80c3-c653767652f0"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (42806-832-01)", "package_ndc": "42806-832-01", "marketing_start_date": "20250313"}], "brand_name": "Buspirone Hydrochloride", "product_id": "42806-832_160f52d2-2e08-4969-80c3-c653767652f0", "dosage_form": "CAPSULE", "product_ndc": "42806-832", "generic_name": "Buspirone Hydrochloride", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE", "strength": "10 mg/1"}], "application_number": "ANDA218628", "marketing_category": "ANDA", "marketing_start_date": "20250313", "listing_expiration_date": "20261231"}