Package 73473-901-05

Brand: neomycin sulfate

Generic: neomycin sulfate
NDC Package

Package Facts

Identity

Package NDC 73473-901-05
Digits Only 7347390105
Product NDC 73473-901
Product ID 73473-901_40441079-4a76-b56f-e063-6394a90a5765
Description

100 TABLET in 1 BOTTLE, PLASTIC (73473-901-05)

Marketing

Marketing Status
Marketed Since 2023-06-01
Brand neomycin sulfate
Generic neomycin sulfate
Sample Package No

Linked Drug Pages (1)

Neomycin Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40441079-4a76-b56f-e063-6394a90a5765", "openfda": {"unii": ["057Y626693"], "rxcui": ["866042"], "spl_set_id": ["f430c5d9-ae82-3314-e053-2a95a90af04c"], "manufacturer_name": ["Solaris Pharma Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (73473-901-05)", "package_ndc": "73473-901-05", "marketing_start_date": "20230601"}], "brand_name": "Neomycin Sulfate", "product_id": "73473-901_40441079-4a76-b56f-e063-6394a90a5765", "dosage_form": "TABLET", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "73473-901", "generic_name": "Neomycin Sulfate", "labeler_name": "Solaris Pharma Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neomycin Sulfate", "active_ingredients": [{"name": "NEOMYCIN SULFATE", "strength": "500 mg/1"}], "application_number": "ANDA065220", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}