Package 25021-198-99

Brand: nafcillin

Generic: nafcillin sodium
NDC Package

Package Facts

Identity

Package NDC 25021-198-99
Digits Only 2502119899
Product NDC 25021-198
Product ID 25021-198_f50e7f65-8bca-4df1-bff1-8069b33def90
Description

1 VIAL in 1 CARTON (25021-198-99) / 100 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2025-04-15
Brand nafcillin
Generic nafcillin sodium
Sample Package No

Linked Drug Pages (1)

Nafcillin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "f50e7f65-8bca-4df1-bff1-8069b33def90", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["239189"], "spl_set_id": ["a6a4e122-b7f5-4eb5-8555-7aea6eda794b"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-198-99)  / 100 mL in 1 VIAL", "package_ndc": "25021-198-99", "marketing_start_date": "20250415"}], "brand_name": "Nafcillin", "product_id": "25021-198_f50e7f65-8bca-4df1-bff1-8069b33def90", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "25021-198", "generic_name": "Nafcillin Sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nafcillin", "active_ingredients": [{"name": "NAFCILLIN SODIUM", "strength": "10 g/100mL"}], "application_number": "ANDA090005", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}