Package 51655-015-52

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-015-52
Digits Only 5165501552
Product NDC 51655-015
Description

30 TABLET in 1 BOTTLE, DISPENSING (51655-015-52)

Marketing

Marketing Status
Marketed Since 2015-02-25
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": "46ddaa45-1fdf-f562-e063-6394a90ac7e8", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["ff02c7cb-f96a-4a3b-99a2-812cd78b345c"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-015-26)", "package_ndc": "51655-015-26", "marketing_start_date": "20230612"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, DISPENSING (51655-015-52)", "package_ndc": "51655-015-52", "marketing_start_date": "20150225"}], "brand_name": "Buspirone Hydrochloride", "product_id": "51655-015_46ddaa45-1fdf-f562-e063-6394a90ac7e8", "dosage_form": "TABLET", "product_ndc": "51655-015", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20150225", "listing_expiration_date": "20261231"}