Package 63323-136-10

Brand: bleomycin

Generic: bleomycin sulfate
NDC Package

Package Facts

Identity

Package NDC 63323-136-10
Digits Only 6332313610
Product NDC 63323-136
Product ID 63323-136_93aba071-101f-4610-90fa-27e3635b2c1c
Description

1 VIAL in 1 CARTON (63323-136-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2009-02-13
Brand bleomycin
Generic bleomycin sulfate
Sample Package No

Linked Drug Pages (1)

Bleomycin ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAPLEURAL", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "93aba071-101f-4610-90fa-27e3635b2c1c", "openfda": {"unii": ["7DP3NTV15T"], "rxcui": ["1726673", "1726676"], "spl_set_id": ["b5806c40-12ce-48e3-8abd-9f8997ef4428"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-136-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "63323-136-10", "marketing_start_date": "20090213"}], "brand_name": "Bleomycin", "product_id": "63323-136_93aba071-101f-4610-90fa-27e3635b2c1c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "63323-136", "generic_name": "BLEOMYCIN SULFATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bleomycin", "active_ingredients": [{"name": "BLEOMYCIN SULFATE", "strength": "15 [USP'U]/1"}], "application_number": "ANDA065185", "marketing_category": "ANDA", "marketing_start_date": "20090213", "listing_expiration_date": "20261231"}