Package 70860-119-99

Brand: nafcillin

Generic: nafcillin sodium
NDC Package

Package Facts

Identity

Package NDC 70860-119-99
Digits Only 7086011999
Product NDC 70860-119
Description

1 BOTTLE in 1 CARTON (70860-119-99) / 100 mL in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2026-06-30
Brand nafcillin
Generic nafcillin sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2cc9cc61-54ac-9a94-e063-6394a90a2376", "openfda": {"unii": ["49G3001BCK"], "rxcui": ["239189"], "spl_set_id": ["2bc91eeb-5d8d-4058-b16a-532ba114fcd5"], "manufacturer_name": ["Athenex Pharmaceutical Division, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70860-119-99)  / 100 mL in 1 BOTTLE", "package_ndc": "70860-119-99", "marketing_end_date": "20260630", "marketing_start_date": "20180815"}], "brand_name": "Nafcillin", "product_id": "70860-119_2cc9cc61-54ac-9a94-e063-6394a90a2376", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]"], "product_ndc": "70860-119", "generic_name": "nafcillin sodium", "labeler_name": "Athenex Pharmaceutical Division, LLC.", "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_end_date": "20260630", "marketing_start_date": "20180815"}