Package 0054-3505-47

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-3505-47
Digits Only 0054350547
Product NDC 0054-3505
Description

50 mL in 1 BOTTLE (0054-3505-47)

Marketing

Marketing Status
Marketed Since 1985-04-03
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3996fa01-1f0c-41ab-8dc3-9a28246138c8", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010878"], "spl_set_id": ["c5d27da0-e495-4bb6-a7e1-8eaa6595eb71"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (0054-3505-47)", "package_ndc": "0054-3505-47", "marketing_start_date": "19850403"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "0054-3505_3996fa01-1f0c-41ab-8dc3-9a28246138c8", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0054-3505", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA088803", "marketing_category": "ANDA", "marketing_start_date": "19850403", "listing_expiration_date": "20261231"}