Package 68788-8507-1

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8507-1
Digits Only 6878885071
Product NDC 68788-8507
Description

100 mL in 1 BOTTLE (68788-8507-1)

Marketing

Marketing Status
Marketed Since 2023-08-16
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL", "TOPICAL"], "spl_id": "4aee6a9c-0a4b-41c6-a6ff-a9b3d4f1f620", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["55aa77b8-7601-4432-8631-bfec58daf247"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8507-1)", "package_ndc": "68788-8507-1", "marketing_start_date": "20230816"}], "brand_name": "Lidocaine hydrochloride", "product_id": "68788-8507_4aee6a9c-0a4b-41c6-a6ff-a9b3d4f1f620", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "68788-8507", "generic_name": "Lidocaine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA216780", "marketing_category": "ANDA", "marketing_start_date": "20230816", "listing_expiration_date": "20261231"}