Package 14789-900-02

Brand: procainamide hydrochloride

Generic: procainamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 14789-900-02
Digits Only 1478990002
Product NDC 14789-900
Product ID 14789-900_44fbdf17-cfd1-0076-e063-6394a90abf0d
Description

10 VIAL, MULTI-DOSE in 1 CARTON (14789-900-02) / 2 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2007-10-14
Brand procainamide hydrochloride
Generic procainamide hydrochloride
Sample Package No

Linked Drug Pages (1)

Procainamide Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "44fbdf17-cfd1-0076-e063-6394a90abf0d", "openfda": {"unii": ["SI4064O0LX"], "rxcui": ["857886", "857962"], "spl_set_id": ["d58751df-cd8b-45a6-8a32-af19e747e23a"], "manufacturer_name": ["Nexus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (14789-900-02)  / 2 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "14789-900-02", "marketing_start_date": "20071014"}], "brand_name": "Procainamide Hydrochloride", "product_id": "14789-900_44fbdf17-cfd1-0076-e063-6394a90abf0d", "dosage_form": "INJECTION", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "14789-900", "generic_name": "Procainamide Hydrochloride", "labeler_name": "Nexus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procainamide Hydrochloride", "active_ingredients": [{"name": "PROCAINAMIDE HYDROCHLORIDE", "strength": "500 mg/mL"}], "application_number": "ANDA206332", "marketing_category": "ANDA", "marketing_start_date": "20071014", "listing_expiration_date": "20261231"}