Package 0378-1150-01

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0378-1150-01
Digits Only 0378115001
Product NDC 0378-1150
Product ID 0378-1150_bf3ebca4-75bb-4f84-a906-06a1337e190f
Description

100 TABLET in 1 BOTTLE, PLASTIC (0378-1150-01)

Marketing

Marketing Status
Discontinued 2026-05-31
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": "bf3ebca4-75bb-4f84-a906-06a1337e190f", "openfda": {"upc": ["0303781150019", "0303781165914", "0303781145015", "0303781175913", "0303781140010"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094", "866111"], "spl_set_id": ["7c9eafb9-9ce1-4b28-900c-8fcb4b23424e"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0378-1150-01)", "package_ndc": "0378-1150-01", "marketing_end_date": "20260531", "marketing_start_date": "20020321"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0378-1150-05)", "package_ndc": "0378-1150-05", "marketing_start_date": "20020321"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0378-1150_bf3ebca4-75bb-4f84-a906-06a1337e190f", "dosage_form": "TABLET", "product_ndc": "0378-1150", "generic_name": "buspirone hydrochloride", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076008", "marketing_category": "ANDA", "marketing_start_date": "20020321", "listing_expiration_date": "20271231"}