Package 11788-061-05

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11788-061-05
Digits Only 1178806105
Product NDC 11788-061
Product ID 11788-061_fe9868fd-eb67-48a4-99a3-f25125507e36
Description

500 TABLET in 1 BOTTLE (11788-061-05)

Marketing

Marketing Status
Marketed Since 2025-09-26
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Buspirone hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fe9868fd-eb67-48a4-99a3-f25125507e36", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["55810b17-4796-49d0-90e4-8e075d62eda4"], "manufacturer_name": ["AiPing Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (11788-061-05)", "package_ndc": "11788-061-05", "marketing_start_date": "20250926"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (11788-061-60)", "package_ndc": "11788-061-60", "marketing_start_date": "20250926"}], "brand_name": "Buspirone hydrochloride", "product_id": "11788-061_fe9868fd-eb67-48a4-99a3-f25125507e36", "dosage_form": "TABLET", "product_ndc": "11788-061", "generic_name": "Buspirone hydrochloride", "labeler_name": "AiPing Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20250926", "listing_expiration_date": "20261231"}