Package 51662-1551-3
Brand: lidocaine hydrochloride
Generic: lidocaine hydrochloridePackage Facts
Identity
Package NDC
51662-1551-3
Digits Only
5166215513
Product NDC
51662-1551
Description
25 POUCH in 1 CASE (51662-1551-3) / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1551-2) / 20 mL in 1 VIAL, SINGLE-USE
Marketing
Marketing Status
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": "10356612-76d5-72cf-e063-6394a90a1ecb", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1011852"], "spl_set_id": ["c4bf5905-add7-1cb0-e053-2995a90a7334"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1551-3) / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1551-2) / 20 mL in 1 VIAL, SINGLE-USE", "package_ndc": "51662-1551-3", "marketing_start_date": "20210614"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "51662-1551_10356612-76d5-72cf-e063-6394a90a1ecb", "dosage_form": "JELLY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51662-1551", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA086283", "marketing_category": "ANDA", "marketing_start_date": "20210614", "listing_expiration_date": "20261231"}