Package 63323-202-02

Brand: lidocaine

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-202-02
Digits Only 6332320202
Product NDC 63323-202
Description

25 VIAL in 1 TRAY (63323-202-02) / 2 mL in 1 VIAL (63323-202-01)

Marketing

Marketing Status
Marketed Since 2010-05-27
Brand lidocaine
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "d19c26f4-1214-40f7-9680-43c885613306", "openfda": {"upc": ["0363323202019", "0363323201036", "0363323201012"], "unii": ["V13007Z41A"], "rxcui": ["1010033", "1737757"], "spl_set_id": ["cddb2b22-fce3-8967-6e54-dca3df5ac4b3"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (63323-202-02)  / 2 mL in 1 VIAL (63323-202-01)", "package_ndc": "63323-202-02", "marketing_start_date": "20100527"}], "brand_name": "Lidocaine", "product_id": "63323-202_d19c26f4-1214-40f7-9680-43c885613306", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "63323-202", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA088586", "marketing_category": "ANDA", "marketing_start_date": "20100527", "listing_expiration_date": "20261231"}