neomycin sulfate

Generic: neomycin sulfate

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name neomycin sulfate
Generic Name neomycin sulfate
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

neomycin sulfate 500 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-1177
Product ID 0093-1177_18e9e5b7-e08c-445e-86bb-90bc0953eda9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA060304
Listing Expiration 2026-12-31
Marketing Start 1990-09-30

Pharmacologic Class

Classes
aminoglycoside antibacterial [epc] aminoglycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00931177
Hyphenated Format 0093-1177

Supplemental Identifiers

RxCUI
866042
UPC
0300931177018
UNII
057Y626693

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name neomycin sulfate (source: ndc)
Generic Name neomycin sulfate (source: ndc)
Application Number ANDA060304 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0093-1177-01)
source: ndc

Packages (1)

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

Ingredients (1)

neomycin sulfate (500 mg/1)

Linked Drug Pages (1)

Neomycin Sulfate ndc-match (0.9)

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"}