Package 0409-1902-01
Brand: procainamide hydrochloride
Generic: procainamide hydrochloridePackage Facts
Identity
Package NDC
0409-1902-01
Digits Only
0409190201
Product NDC
0409-1902
Description
25 CARTON in 1 CASE (0409-1902-01) / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1902-11) / 10 mL in 1 VIAL, MULTI-DOSE
Marketing
Marketing Status
Brand
procainamide hydrochloride
Generic
procainamide hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "5c75003d-8b7f-4e26-b76e-11a749a53ae6", "openfda": {"unii": ["SI4064O0LX"], "rxcui": ["857886"], "spl_set_id": ["17e47845-daad-434c-a784-6d3875b0d704"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 CARTON in 1 CASE (0409-1902-01) / 1 VIAL, MULTI-DOSE in 1 CARTON (0409-1902-11) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0409-1902-01", "marketing_start_date": "20060308"}], "brand_name": "Procainamide Hydrochloride", "product_id": "0409-1902_5c75003d-8b7f-4e26-b76e-11a749a53ae6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "0409-1902", "generic_name": "PROCAINAMIDE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procainamide Hydrochloride", "active_ingredients": [{"name": "PROCAINAMIDE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA089069", "marketing_category": "ANDA", "marketing_start_date": "20060308", "listing_expiration_date": "20271231"}