mitomycin

Generic: mitomycin

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mitomycin
Generic Name mitomycin
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

mitomycin 20 mg/40mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-251
Product ID 25021-251_865914d0-b74e-4beb-a7d1-e31a82b75c05
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215687
Listing Expiration 2026-12-31
Marketing Start 2023-06-15

Pharmacologic Class

Established (EPC)
alkylating drug [epc]
Mechanism of Action
alkylating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021251
Hyphenated Format 25021-251

Supplemental Identifiers

RxCUI
1740894 1740900
UNII
50SG953SK6
NUI
N0000000236 N0000175558

Packaging Origin

Original Packager
true

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 mitomycin (source: ndc)
Generic Name mitomycin (source: ndc)
Application Number ANDA215687 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/40mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (25021-251-50) / 40 mL in 1 VIAL
source: ndc

Packages (1)

25021-251-50 1 VIAL in 1 CARTON (25021-251-50) / 40 mL in 1 VIAL

Ingredients (1)

mitomycin (20 mg/40mL)

Linked Drug Pages (1)

Mitomycin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "865914d0-b74e-4beb-a7d1-e31a82b75c05", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["50SG953SK6"], "rxcui": ["1740894", "1740900"], "spl_set_id": ["10c41a58-c305-4240-80d2-caa070412648"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-251-50)  / 40 mL in 1 VIAL", "package_ndc": "25021-251-50", "marketing_start_date": "20230615"}], "brand_name": "Mitomycin", "product_id": "25021-251_865914d0-b74e-4beb-a7d1-e31a82b75c05", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "25021-251", "generic_name": "Mitomycin", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mitomycin", "active_ingredients": [{"name": "MITOMYCIN", "strength": "20 mg/40mL"}], "application_number": "ANDA215687", "marketing_category": "ANDA", "marketing_start_date": "20230615", "listing_expiration_date": "20261231"}