Package 0078-0813-01

Brand: tobrex

Generic: tobramycin
NDC Package

Package Facts

Identity

Package NDC 0078-0813-01
Digits Only 0078081301
Product NDC 0078-0813
Description

3.5 g in 1 TUBE (0078-0813-01)

Marketing

Marketing Status
Marketed Since 2022-03-08
Brand tobrex
Generic tobramycin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "5e274c59-a22a-43a1-a3bd-b4f128dbee31", "openfda": {"nui": ["N0000175477", "M0000946"], "unii": ["VZ8RRZ51VK"], "rxcui": ["207850", "313414"], "spl_set_id": ["5b66bba3-cf97-4a9c-b618-ba5f277f20f6"], "pharm_class_cs": ["Aminoglycosides [CS]"], "pharm_class_epc": ["Aminoglycoside Antibacterial [EPC]"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3.5 g in 1 TUBE (0078-0813-01)", "package_ndc": "0078-0813-01", "marketing_start_date": "20220308"}], "brand_name": "TOBREX", "product_id": "0078-0813_5e274c59-a22a-43a1-a3bd-b4f128dbee31", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "0078-0813", "generic_name": "tobramycin", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TOBREX", "active_ingredients": [{"name": "TOBRAMYCIN", "strength": "3 mg/g"}], "application_number": "NDA050555", "marketing_category": "NDA", "marketing_start_date": "19810628", "listing_expiration_date": "20261231"}