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United States · US · US:69448-003_302614d9-cc10-737a-e063-6294a90a41c3
MUTAMYCIN
Orange BookUNIISPLATC L01DC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAccord BioPharma Inc.
CountryUS (United States)
ATC codeL01DC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169448003381 VIAL in 1 BOX, UNIT-DOSE (69448-003-38) / 80 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
50SG953SK6
MITOMYCIN
RxCUI 632
Orange Book
A064144
APAPAP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "50SG953SK6",
"rxcui": "632",
"inchikey": "NWIBSHFKIJFRCO-WUDYKRTCSA-N",
"display_name": "MITOMYCIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"cbf0f6ba-3a53-4791-9a85-5c6b271eeb8e": {
"match": "brand_token",
"title": "MUTAMYCIN (MITOMYCIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ACCORD BIOPHARMA INC.]",
"spl_version": "3",
"published_date": "2025-03-17"
}
},
"productid": "69448-003_302614d9-cc10-737a-e063-6294a90a41c3",
"productndc": "69448-003",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "064144",
"products": [
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "5MG/VIAL",
"product_no": "001",
"approval_date": "Apr 30, 1998"
},
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "20MG/VIAL",
"product_no": "002",
"approval_date": "Apr 30, 1998"
},
{
"rs": true,
"rld": false,
"te_code": "AP",
"strength": "40MG/VIAL",
"product_no": "003",
"approval_date": "Aug 11, 2009"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "MITOMYCIN",
"proprietary_name": "MUTAMYCIN",
"active_ingred_unit": "mg/80mL",
"application_number": "ANDA064144",
"marketing_category": "ANDA",
"nonproprietary_name": "Mitomycin",
"start_marketing_date": "20170725",
"active_numerator_strength": "40"
}Related drugs
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