mitomycin

Generic: mitomycin

Labeler: bluepoint laboratories
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

mitomycin 40 mg/80mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-391
Product ID 68001-391_c455e123-6115-d234-e053-2995a90a2e93
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA064144
Listing Expiration 2026-12-31
Marketing Start 2019-05-14

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 68001391
Hyphenated Format 68001-391

Supplemental Identifiers

RxCUI
1740894 1740898 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 ANDA064144 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/80mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX, UNIT-DOSE (68001-391-79) / 80 mL in 1 VIAL (68001-391-80)
source: ndc

Packages (1)

68001-391-79 1 VIAL in 1 BOX, UNIT-DOSE (68001-391-79) / 80 mL in 1 VIAL (68001-391-80)

Ingredients (1)

mitomycin (40 mg/80mL)

Linked Drug Pages (1)

Mitomycin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c455e123-6115-d234-e053-2995a90a2e93", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["50SG953SK6"], "rxcui": ["1740894", "1740898", "1740900"], "spl_set_id": ["aad9a9a0-7204-452a-8b9b-6d625c4ee021"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (68001-391-79)  / 80 mL in 1 VIAL (68001-391-80)", "package_ndc": "68001-391-79", "marketing_start_date": "20190514"}], "brand_name": "Mitomycin", "product_id": "68001-391_c455e123-6115-d234-e053-2995a90a2e93", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "68001-391", "generic_name": "Mitomycin", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mitomycin", "active_ingredients": [{"name": "MITOMYCIN", "strength": "40 mg/80mL"}], "application_number": "ANDA064144", "marketing_category": "ANDA", "marketing_start_date": "20190514", "listing_expiration_date": "20261231"}