Package 0121-0972-51

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-0972-51
Digits Only 0121097251
Product NDC 0121-0972
Description

1 BOTTLE, GLASS in 1 CARTON (0121-0972-51) / 50 mL in 1 BOTTLE, GLASS

Marketing

Marketing Status
Marketed Since 2023-07-31
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": "a8761ec7-33e3-43fe-bb07-5e6144a8926e", "openfda": {"upc": ["0301210972515"], "unii": ["V13007Z41A"], "rxcui": ["1010878"], "spl_set_id": ["9920daef-b156-4a14-b641-f714191ffb5c"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (0121-0972-51)  / 50 mL in 1 BOTTLE, GLASS", "package_ndc": "0121-0972-51", "marketing_start_date": "20230731"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "0121-0972_a8761ec7-33e3-43fe-bb07-5e6144a8926e", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0121-0972", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA204494", "marketing_category": "ANDA", "marketing_start_date": "20230731", "listing_expiration_date": "20261231"}