bleomycin
Generic: bleomycin
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
bleomycin
Generic Name
bleomycin
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
bleomycin sulfate 15 [USP'U]/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9240
Product ID
0143-9240_c8047994-3b3a-4e16-809b-786e47014fe9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065042
Listing Expiration
2026-12-31
Marketing Start
2018-01-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439240
Hyphenated Format
0143-9240
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 (source: ndc)
Application Number
ANDA065042 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 15 [USP'U]/1
Packaging
- 1 VIAL in 1 BOX, UNIT-DOSE (0143-9240-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
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": "c8047994-3b3a-4e16-809b-786e47014fe9", "openfda": {"unii": ["7DP3NTV15T"], "rxcui": ["1726673", "1726676"], "spl_set_id": ["cccfb763-79fa-4186-89fb-d8d061d3c161"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9240-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9240-01", "marketing_start_date": "20180109"}], "brand_name": "Bleomycin", "product_id": "0143-9240_c8047994-3b3a-4e16-809b-786e47014fe9", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "0143-9240", "generic_name": "Bleomycin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bleomycin", "active_ingredients": [{"name": "BLEOMYCIN SULFATE", "strength": "15 [USP'U]/1"}], "application_number": "ANDA065042", "marketing_category": "ANDA", "marketing_start_date": "20180109", "listing_expiration_date": "20261231"}