neomycin sulfate

Generic: neomycin sulfate

Labeler: solaris pharma corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name neomycin sulfate
Generic Name neomycin sulfate
Labeler solaris pharma corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

neomycin sulfate 500 mg/1

Manufacturer
Solaris Pharma Corporation

Identifiers & Regulatory

Product NDC 73473-901
Product ID 73473-901_40441079-4a76-b56f-e063-6394a90a5765
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065220
Listing Expiration 2026-12-31
Marketing Start 2023-06-01

Pharmacologic Class

Classes
aminoglycoside antibacterial [epc] aminoglycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 73473901
Hyphenated Format 73473-901

Supplemental Identifiers

RxCUI
866042
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 ANDA065220 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (73473-901-05)
source: ndc

Packages (1)

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

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": "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"}