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United States · US · US:51672-1370_4f1deb92-5055-69e7-e063-6394a90a40bb
Mupirocin
Orange BookUNIISPLATC D06AX09
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeD06AX09
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1151672137011 TUBE in 1 CARTON (51672-1370-1) / 15 g in 1 TUBE
- ndc1151672137021 TUBE in 1 CARTON (51672-1370-2) / 30 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
RG38I2P540
MUPIROCIN CALCIUM
RxCUI 221128
Orange Book
A207116
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "RG38I2P540",
"rxcui": "221128",
"inchikey": "DDHVILIIHBIMQU-YJGQQKNPSA-L",
"display_name": "MUPIROCIN CALCIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"c70dd5d7-6995-4a3d-b19c-9b4a2cfe3da9": {
"match": "brand_token",
"title": "MUPIROCIN OINTMENT [SPORTPHARM LLC]",
"spl_version": "1",
"published_date": "2026-05-13"
}
},
"productid": "51672-1370_4f1deb92-5055-69e7-e063-6394a90a40bb",
"productndc": "51672-1370",
"dosage_form": "CREAM",
"orange_book": {
"appl_no": "207116",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 2% BASE",
"product_no": "001",
"approval_date": "Apr 27, 2020"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MUPIROCIN CALCIUM",
"proprietary_name": "Mupirocin",
"active_ingred_unit": "mg/g",
"application_number": "ANDA207116",
"marketing_category": "ANDA",
"nonproprietary_name": "Mupirocin Calcium",
"start_marketing_date": "20200427",
"active_numerator_strength": "20"
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