Package 60687-801-21

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-801-21
Digits Only 6068780121
Product NDC 60687-801
Description

30 BLISTER PACK in 1 CARTON (60687-801-21) / 1 TABLET in 1 BLISTER PACK (60687-801-11)

Marketing

Marketing Status
Marketed Since 2024-02-21
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": "1a4e0770-e1ad-f44a-e063-6294a90a8257", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866111"], "spl_set_id": ["e80d83a6-7c2a-478e-bdf1-c481824fc301"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (60687-801-21)  / 1 TABLET in 1 BLISTER PACK (60687-801-11)", "package_ndc": "60687-801-21", "marketing_start_date": "20240221"}], "brand_name": "Buspirone hydrochloride", "product_id": "60687-801_1a4e0770-e1ad-f44a-e063-6294a90a8257", "dosage_form": "TABLET", "product_ndc": "60687-801", "generic_name": "Buspirone hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20240221", "listing_expiration_date": "20261231"}