Package 0404-9887-02
Brand: lidocaine hydrochloride
Generic: lidocaine hydrochloride anhydrousPackage Facts
Identity
Package NDC
0404-9887-02
Digits Only
0404988702
Product NDC
0404-9887
Description
1 AMPULE in 1 BAG (0404-9887-02) / 2 mL in 1 AMPULE
Marketing
Marketing Status
Brand
lidocaine hydrochloride
Generic
lidocaine hydrochloride anhydrous
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION"], "spl_id": "987b167e-430b-4fcc-8d1a-9017504b5849", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737568"], "spl_set_id": ["a5d4b206-cc53-470f-9bca-abfc6ea5cc99"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 AMPULE in 1 BAG (0404-9887-02) / 2 mL in 1 AMPULE", "package_ndc": "0404-9887-02", "marketing_start_date": "20220112"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "0404-9887_987b167e-430b-4fcc-8d1a-9017504b5849", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0404-9887", "generic_name": "Lidocaine Hydrochloride Anhydrous", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA080408", "marketing_category": "ANDA", "marketing_start_date": "20220112", "listing_expiration_date": "20261231"}