bleomycin
Generic: bleomycin sulfate
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
bleomycin
Generic Name
bleomycin sulfate
Labeler
meitheal pharmaceuticals inc.
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
bleomycin sulfate 15 [USP'U]/1
Manufacturer
Identifiers & Regulatory
Product NDC
71288-106
Product ID
71288-106_ae0d7fba-937e-42d1-b7f5-ae6f7b860bc4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205030
Listing Expiration
2026-12-31
Marketing Start
2018-08-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288106
Hyphenated Format
71288-106
Supplemental Identifiers
RxCUI
UNII
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
bleomycin (source: ndc)
Generic Name
bleomycin sulfate (source: ndc)
Application Number
ANDA205030 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 [USP'U]/1
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-106-10) / 15 POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAPLEURAL", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "ae0d7fba-937e-42d1-b7f5-ae6f7b860bc4", "openfda": {"unii": ["7DP3NTV15T"], "rxcui": ["1726673", "1726676"], "spl_set_id": ["640602f9-a7df-46f0-a9b1-19c471008bee"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-106-10) / 15 POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-106-10", "marketing_start_date": "20180831"}], "brand_name": "Bleomycin", "product_id": "71288-106_ae0d7fba-937e-42d1-b7f5-ae6f7b860bc4", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "71288-106", "generic_name": "Bleomycin Sulfate", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bleomycin", "active_ingredients": [{"name": "BLEOMYCIN SULFATE", "strength": "15 [USP'U]/1"}], "application_number": "ANDA205030", "marketing_category": "ANDA", "marketing_start_date": "20180831", "listing_expiration_date": "20261231"}