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 20 mg/40mL

Manufacturer
BluePoint Laboratories

Identifiers & Regulatory

Product NDC 68001-616
Product ID 68001-616_2094e27c-5df6-5cb8-e063-6294a90ae690
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216732
Listing Expiration 2026-12-31
Marketing Start 2024-06-24

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 68001616
Hyphenated Format 68001-616

Supplemental Identifiers

RxCUI
1740894 1740898 1740900
UPC
0368001617796 0368001616775 0368001615365
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 ANDA216732 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/40mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-616-77) / 40 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

mitomycin (20 mg/40mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2094e27c-5df6-5cb8-e063-6294a90ae690", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0368001617796", "0368001616775", "0368001615365"], "unii": ["50SG953SK6"], "rxcui": ["1740894", "1740898", "1740900"], "spl_set_id": ["57129df7-d6b1-419e-90ec-54f9b5182e7c"], "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, SINGLE-DOSE in 1 CARTON (68001-616-77)  / 40 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-616-77", "marketing_start_date": "20240624"}], "brand_name": "MITOMYCIN", "product_id": "68001-616_2094e27c-5df6-5cb8-e063-6294a90ae690", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "68001-616", "generic_name": "MITOMYCIN", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MITOMYCIN", "active_ingredients": [{"name": "MITOMYCIN", "strength": "20 mg/40mL"}], "application_number": "ANDA216732", "marketing_category": "ANDA", "marketing_start_date": "20240624", "listing_expiration_date": "20261231"}