mitomycin
Generic: mitomycin
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
mitomycin
Generic Name
mitomycin
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
mitomycin 40 mg/80mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-139
Product ID
71288-139_968a3675-c8a8-477c-ad1d-bc8741fa6a6e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214504
Listing Expiration
2026-12-31
Marketing Start
2022-09-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288139
Hyphenated Format
71288-139
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA214504 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/80mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-139-51) / 80 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "968a3675-c8a8-477c-ad1d-bc8741fa6a6e", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["50SG953SK6"], "rxcui": ["1740898"], "spl_set_id": ["eae9a8bc-84ec-4303-bc43-f656a5ce0fb7"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-139-51) / 80 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-139-51", "marketing_start_date": "20220906"}], "brand_name": "MITOMYCIN", "product_id": "71288-139_968a3675-c8a8-477c-ad1d-bc8741fa6a6e", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "71288-139", "generic_name": "MITOMYCIN", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MITOMYCIN", "active_ingredients": [{"name": "MITOMYCIN", "strength": "40 mg/80mL"}], "application_number": "ANDA214504", "marketing_category": "ANDA", "marketing_start_date": "20220906", "listing_expiration_date": "20261231"}