Package 71288-726-52

Brand: bupivacaine hydrochloride

Generic: bupivacaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71288-726-52
Digits Only 7128872652
Product NDC 71288-726
Description

1 VIAL, MULTI-DOSE in 1 CARTON (71288-726-52) / 50 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2023-06-23
Brand bupivacaine hydrochloride
Generic bupivacaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["PERINEURAL"], "spl_id": "0949c302-51ce-4fc9-8b99-1df94e693718", "openfda": {"unii": ["7TQO7W3VT8"], "rxcui": ["1012396", "1012404"], "spl_set_id": ["fe340f98-a0f3-446e-b281-47fd91c1e537"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (71288-726-52)  / 50 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71288-726-52", "marketing_start_date": "20230623"}], "brand_name": "bupivacaine hydrochloride", "product_id": "71288-726_0949c302-51ce-4fc9-8b99-1df94e693718", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "71288-726", "generic_name": "bupivacaine hydrochloride", "labeler_name": "Meitheal Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupivacaine hydrochloride", "active_ingredients": [{"name": "BUPIVACAINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA216039", "marketing_category": "ANDA", "marketing_start_date": "20230623", "listing_expiration_date": "20261231"}