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United States · US · US:0093-1177_18e9e5b7-e08c-445e-86bb-90bc0953eda9
Neomycin Sulfate
Orange BookUNIISPLATC R02AB01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTeva Pharmaceuticals USA, Inc.
CountryUS (United States)
ATC codeR02AB01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110093117701100 TABLET in 1 BOTTLE (0093-1177-01)
Annotations
UNII (FDA Substance ID)
057Y626693
NEOMYCIN SULFATE
RxCUI 7300
Orange Book
A060304
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "057Y626693",
"rxcui": "7300",
"inchikey": null,
"display_name": "NEOMYCIN SULFATE",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"a2f47d77-efd3-4c84-a364-08fb6d9978eb": {
"match": "brand_token",
"title": "NEOMYCIN AND POLYMYXIN B SULFATES SOLUTION [XGEN PHARMACEUTICALS DJB, INC.]",
"spl_version": "18",
"published_date": "2026-05-21"
}
},
"productid": "0093-1177_18e9e5b7-e08c-445e-86bb-90bc0953eda9",
"productndc": "0093-1177",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "060304",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AA",
"strength": "500MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "NEOMYCIN SULFATE",
"proprietary_name": "Neomycin Sulfate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA060304",
"marketing_category": "ANDA",
"nonproprietary_name": "Neomycin Sulfate",
"start_marketing_date": "19900930",
"active_numerator_strength": "500"
}Related drugs
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