Package 16714-908-01
Brand: bleomycin
Generic: bleomycinPackage Facts
Identity
Package NDC
16714-908-01
Digits Only
1671490801
Product NDC
16714-908
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (16714-908-01) / 30 POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
bleomycin
Generic
bleomycin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAPLEURAL", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "f202dd8d-b51c-4544-a952-8a3acfd71c95", "openfda": {"upc": ["0316714908014"], "unii": ["7DP3NTV15T"], "rxcui": ["1726673", "1726676"], "spl_set_id": ["6824b1e1-e5fa-4371-ade9-1346e12ab0c7"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (16714-908-01) / 30 POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "16714-908-01", "marketing_start_date": "20181201"}], "brand_name": "Bleomycin", "product_id": "16714-908_f202dd8d-b51c-4544-a952-8a3acfd71c95", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cytoprotective Agent [EPC]"], "product_ndc": "16714-908", "generic_name": "Bleomycin", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bleomycin", "active_ingredients": [{"name": "BLEOMYCIN SULFATE", "strength": "30 [USP'U]/1"}], "application_number": "ANDA205030", "marketing_category": "ANDA", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}