Package 85766-013-10

Brand: bupivacaine hydrochloride

Generic: bupivacaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 85766-013-10
Digits Only 8576601310
Product NDC 85766-013
Description

10 mL in 1 VIAL, SINGLE-DOSE (85766-013-10)

Marketing

Marketing Status
Marketed Since 2025-06-20
Brand bupivacaine hydrochloride
Generic bupivacaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INTRACAUDAL", "PERINEURAL"], "spl_id": "49eeda32-7627-4c62-e063-6394a90af3eb", "openfda": {"unii": ["7TQO7W3VT8"], "rxcui": ["1724880"], "spl_set_id": ["0e6a55f0-5107-4ea9-9ee1-5c6c09bbe4a6"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (85766-013-10)", "package_ndc": "85766-013-10", "marketing_start_date": "20250620"}], "brand_name": "Bupivacaine Hydrochloride", "product_id": "85766-013_49eeda32-7627-4c62-e063-6394a90af3eb", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "85766-013", "generic_name": "BUPIVACAINE HYDROCHLORIDE", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupivacaine Hydrochloride", "active_ingredients": [{"name": "BUPIVACAINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA070584", "marketing_category": "ANDA", "marketing_start_date": "20051122", "listing_expiration_date": "20271231"}