Package 10135-736-51

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10135-736-51
Digits Only 1013573651
Product NDC 10135-736
Product ID 10135-736_4260de8c-7ec7-00d0-e063-6394a90aeebd
Description

1 BOTTLE in 1 CARTON (10135-736-51) / 50 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2022-06-01
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": ["TOPICAL"], "spl_id": "4260de8c-7ec7-00d0-e063-6394a90aeebd", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010878"], "spl_set_id": ["e1badbba-59af-e451-e053-2a95a90a49f8"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (10135-736-51)  / 50 mL in 1 BOTTLE", "package_ndc": "10135-736-51", "marketing_start_date": "20220601"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "10135-736_4260de8c-7ec7-00d0-e063-6394a90aeebd", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "10135-736", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA216250", "marketing_category": "ANDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}