Package 25021-323-02

Brand: procainamide hydrochloride

Generic: procainamide hydrochloride
NDC Package

Package Facts

Identity

Package NDC 25021-323-02
Digits Only 2502132302
Product NDC 25021-323
Description

10 VIAL in 1 CARTON (25021-323-02) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-01-15
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": "65bd5a24-3fbb-4264-b26f-5839143936db", "openfda": {"unii": ["SI4064O0LX"], "rxcui": ["857886", "857962"], "spl_set_id": ["358c956e-8c6c-4bd6-a6bc-194d5b3d6d9a"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-323-02)  / 2 mL in 1 VIAL", "package_ndc": "25021-323-02", "marketing_start_date": "20250115"}], "brand_name": "Procainamide Hydrochloride", "product_id": "25021-323_65bd5a24-3fbb-4264-b26f-5839143936db", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "25021-323", "generic_name": "Procainamide Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Procainamide Hydrochloride", "active_ingredients": [{"name": "PROCAINAMIDE HYDROCHLORIDE", "strength": "500 mg/mL"}], "application_number": "ANDA218135", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}