Package 36000-242-01

Brand: tobramycin

Generic: tobramycin
NDC Package

Package Facts

Identity

Package NDC 36000-242-01
Digits Only 3600024201
Product NDC 36000-242
Description

1 VIAL, MULTI-DOSE in 1 CARTON (36000-242-01) / 30 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2016-07-15
Brand tobramycin
Generic tobramycin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "19ade85b-3da4-44af-8ad0-d68d15a48193", "openfda": {"upc": ["0336000244015", "0336000242011"], "unii": ["HJT0RXD7JK"], "rxcui": ["597823"], "spl_set_id": ["a9897444-71f6-42af-9b71-4aa77829ade0"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (36000-242-01)  / 30 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "36000-242-01", "marketing_start_date": "20160715"}], "brand_name": "Tobramycin", "product_id": "36000-242_19ade85b-3da4-44af-8ad0-d68d15a48193", "dosage_form": "INJECTION", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "36000-242", "generic_name": "Tobramycin", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tobramycin", "active_ingredients": [{"name": "TOBRAMYCIN SULFATE", "strength": "40 mg/mL"}], "application_number": "ANDA206965", "marketing_category": "ANDA", "marketing_start_date": "20160715", "listing_expiration_date": "20261231"}