Package 82449-504-02

Brand: NAFCILLIN SODIUM

Generic: NAFCILLIN SODIUM
NDC Package

Package Facts

Identity

Package NDC 82449-504-02
Digits Only 8244950402
Product NDC 82449-504
Description

10 VIAL in 1 CARTON (82449-504-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-10-17
Brand NAFCILLIN SODIUM
Generic NAFCILLIN SODIUM
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "07e8b20a-f473-78ed-e063-6394a90a3340", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["1721458", "1721460"], "spl_set_id": ["344455bd-051d-4c4a-b76e-8c4dd9351d97"], "manufacturer_name": ["Steriscience Specialties Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (82449-504-02)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL", "package_ndc": "82449-504-02", "marketing_start_date": "20231017"}], "brand_name": "NAFCILLIN SODIUM", "product_id": "82449-504_07e8b20a-f473-78ed-e063-6394a90a3340", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "82449-504", "generic_name": "NAFCILLIN SODIUM", "labeler_name": "Steriscience Specialties Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAFCILLIN SODIUM", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "2 g/1"}], "application_number": "ANDA200002", "marketing_category": "ANDA", "marketing_start_date": "20231017", "listing_expiration_date": "20261231"}