Package 68071-2987-3

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2987-3
Digits Only 6807129873
Product NDC 68071-2987
Description

30 TABLET in 1 BOTTLE, PLASTIC (68071-2987-3)

Marketing

Marketing Status
Marketed Since 2023-04-17
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": "2dcdccf6-bd84-0ce9-e063-6394a90a0c0e", "openfda": {"upc": ["0368071298734"], "unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["f98d258d-6479-253a-e053-6394a90acbb3"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-2987-3)", "package_ndc": "68071-2987-3", "marketing_start_date": "20230417"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68071-2987_2dcdccf6-bd84-0ce9-e063-6394a90a0c0e", "dosage_form": "TABLET", "product_ndc": "68071-2987", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20191114", "listing_expiration_date": "20261231"}