neomycin sulfate
Generic: neomycin sulfate
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
neomycin sulfate
Generic Name
neomycin sulfate
Labeler
chartwell rx, llc
Dosage Form
TABLET
Routes
Active Ingredients
neomycin sulfate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62135-443
Product ID
62135-443_4bd236cf-36cb-c633-e063-6294a90a5b16
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204435
Listing Expiration
2027-12-31
Marketing Start
2016-06-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135443
Hyphenated Format
62135-443
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA204435 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (62135-443-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bd236cf-36cb-c633-e063-6294a90a5b16", "openfda": {"upc": ["0362135443900"], "unii": ["057Y626693"], "rxcui": ["866042"], "spl_set_id": ["0aa6947b-4739-4b00-be93-7303a5fc687d"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-443-90)", "package_ndc": "62135-443-90", "marketing_start_date": "20231127"}], "brand_name": "Neomycin Sulfate", "product_id": "62135-443_4bd236cf-36cb-c633-e063-6294a90a5b16", "dosage_form": "TABLET", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]"], "product_ndc": "62135-443", "generic_name": "Neomycin Sulfate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neomycin Sulfate", "active_ingredients": [{"name": "NEOMYCIN SULFATE", "strength": "500 mg/1"}], "application_number": "ANDA204435", "marketing_category": "ANDA", "marketing_start_date": "20160610", "listing_expiration_date": "20271231"}