Package 77771-237-60

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 77771-237-60
Digits Only 7777123760
Product NDC 77771-237
Description

60 TABLET in 1 BOTTLE (77771-237-60)

Marketing

Marketing Status
Marketed Since 2025-09-18
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": "3f66a40c-b9b2-06d4-e063-6294a90a9dda", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["3f66a3fe-9d73-180c-e063-6394a90aacca"], "manufacturer_name": ["Radha Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (77771-237-05)", "package_ndc": "77771-237-05", "marketing_start_date": "20250918"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (77771-237-60)", "package_ndc": "77771-237-60", "marketing_start_date": "20250918"}], "brand_name": "Buspirone hydrochloride", "product_id": "77771-237_3f66a40c-b9b2-06d4-e063-6294a90a9dda", "dosage_form": "TABLET", "product_ndc": "77771-237", "generic_name": "Buspirone hydrochloride", "labeler_name": "Radha Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}