Package 84549-162-02
Brand: bupivacaine hydrochloride
Generic: bupivacaine hydrochloridePackage Facts
Identity
Package NDC
84549-162-02
Digits Only
8454916202
Product NDC
84549-162
Description
30 mL in 1 VIAL, SINGLE-DOSE (84549-162-02)
Marketing
Marketing Status
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": "463e0e03-4f19-1b80-e063-6394a90a4da7", "openfda": {"unii": ["7TQO7W3VT8"], "rxcui": ["1724884"], "spl_set_id": ["42c973e2-307b-924c-e063-6394a90a737a"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 VIAL, SINGLE-DOSE (84549-162-02)", "package_ndc": "84549-162-02", "marketing_start_date": "20251010"}], "brand_name": "Bupivacaine Hydrochloride", "product_id": "84549-162_463e0e03-4f19-1b80-e063-6394a90a4da7", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "84549-162", "generic_name": "BUPIVACAINE HYDROCHLORIDE", "labeler_name": "ProPharma Distribution", "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"}