Package 0093-1177-01

Brand: neomycin sulfate

Generic: neomycin sulfate
NDC Package

Package Facts

Identity

Package NDC 0093-1177-01
Digits Only 0093117701
Product NDC 0093-1177
Product ID 0093-1177_18e9e5b7-e08c-445e-86bb-90bc0953eda9
Description

100 TABLET in 1 BOTTLE (0093-1177-01)

Marketing

Marketing Status
Marketed Since 1990-09-30
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": "18e9e5b7-e08c-445e-86bb-90bc0953eda9", "openfda": {"upc": ["0300931177018"], "unii": ["057Y626693"], "rxcui": ["866042"], "spl_set_id": ["777dbfab-f83e-4738-ae1e-78619a9f82a7"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-1177-01)", "package_ndc": "0093-1177-01", "marketing_start_date": "19900930"}], "brand_name": "Neomycin Sulfate", "product_id": "0093-1177_18e9e5b7-e08c-445e-86bb-90bc0953eda9", "dosage_form": "TABLET", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "0093-1177", "generic_name": "Neomycin Sulfate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neomycin Sulfate", "active_ingredients": [{"name": "NEOMYCIN SULFATE", "strength": "500 mg/1"}], "application_number": "ANDA060304", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}