mutamycin

Generic: mitomycin

Labeler: accord biopharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mutamycin
Generic Name mitomycin
Labeler accord biopharma inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

mitomycin 5 mg/10mL

Manufacturer
Accord BioPharma Inc.

Identifiers & Regulatory

Product NDC 69448-001
Product ID 69448-001_302614d9-cc10-737a-e063-6294a90a41c3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA064144
Listing Expiration 2026-12-31
Marketing Start 2017-07-25

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 69448001
Hyphenated Format 69448-001

Supplemental Identifiers

RxCUI
1740894 1740898 1740900 1812480 1812482 1812484
UPC
0369448001056 0369448002114
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 mutamycin (source: ndc)
Generic Name mitomycin (source: ndc)
Application Number ANDA064144 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/10mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (69448-001-05) / 10 mL in 1 VIAL
source: ndc

Packages (1)

69448-001-05 1 VIAL in 1 CARTON (69448-001-05) / 10 mL in 1 VIAL

Ingredients (1)

mitomycin (5 mg/10mL)

Linked Drug Pages (1)

MUTAMYCIN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "302614d9-cc10-737a-e063-6294a90a41c3", "openfda": {"nui": ["N0000000236", "N0000175558"], "upc": ["0369448001056", "0369448002114"], "unii": ["50SG953SK6"], "rxcui": ["1740894", "1740898", "1740900", "1812480", "1812482", "1812484"], "spl_set_id": ["cbf0f6ba-3a53-4791-9a85-5c6b271eeb8e"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Accord BioPharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (69448-001-05)  / 10 mL in 1 VIAL", "package_ndc": "69448-001-05", "marketing_start_date": "20170725"}], "brand_name": "MUTAMYCIN", "product_id": "69448-001_302614d9-cc10-737a-e063-6294a90a41c3", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "69448-001", "generic_name": "Mitomycin", "labeler_name": "Accord BioPharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MUTAMYCIN", "active_ingredients": [{"name": "MITOMYCIN", "strength": "5 mg/10mL"}], "application_number": "ANDA064144", "marketing_category": "ANDA", "marketing_start_date": "20170725", "listing_expiration_date": "20261231"}