Package 76420-579-10

Brand: bupivacaine hydrochloride

Generic: bupivacaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-579-10
Digits Only 7642057910
Product NDC 76420-579
Description

10 mL in 1 VIAL, SINGLE-DOSE (76420-579-10)

Marketing

Marketing Status
Marketed Since 2023-08-09
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": "02772bd6-36ba-d64e-e063-6294a90ab039", "openfda": {"unii": ["7TQO7W3VT8"], "rxcui": ["1724880"], "spl_set_id": ["8759cac8-d977-4c2a-814c-5b59f2f0c910"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (76420-579-10)", "package_ndc": "76420-579-10", "marketing_start_date": "20230809"}], "brand_name": "Bupivacaine Hydrochloride", "product_id": "76420-579_02772bd6-36ba-d64e-e063-6294a90ab039", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "76420-579", "generic_name": "BUPIVACAINE HYDROCHLORIDE", "labeler_name": "Asclemed USA, Inc.", "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": "20261231"}