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United States · US · US:16714-055_4f1f71b7-a564-8070-e063-6394a90a52ca
Mupirocin
Orange BookUNIISPLATC D06AX09
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerNORTHSTAR RX LLC
CountryUS (United States)
ATC codeD06AX09
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1116714055011 TUBE in 1 CARTON (16714-055-01) / 15 g in 1 TUBE
- ndc1116714055021 TUBE in 1 CARTON (16714-055-02) / 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": "16714-055_4f1f71b7-a564-8070-e063-6394a90a52ca",
"productndc": "16714-055",
"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": "20201125",
"active_numerator_strength": "20"
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