Package 17856-8138-1

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17856-8138-1
Digits Only 1785681381
Product NDC 17856-8138
Product ID 17856-8138_401eca82-6f41-2006-e063-6394a90a6421
Description

50 CUP, UNIT-DOSE in 1 CASE (17856-8138-1) / 15 mL in 1 CUP, UNIT-DOSE

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Lidocaine hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "TOPICAL"], "spl_id": "401eca82-6f41-2006-e063-6394a90a6421", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["401ecb6c-392b-1d74-e063-6294a90a4005"], "manufacturer_name": ["Atlantic Biologicals Corp."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (17856-8138-1)  / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-8138-1", "marketing_start_date": "20251001"}], "brand_name": "Lidocaine hydrochloride", "product_id": "17856-8138_401eca82-6f41-2006-e063-6394a90a6421", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "17856-8138", "generic_name": "Lidocaine hydrochloride", "labeler_name": "Atlantic Biologicals Corp.", "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": "20230328", "listing_expiration_date": "20261231"}