Package 43547-632-01
Brand: pemetrexed
Generic: pemetrexedPackage Facts
Identity
Package NDC
43547-632-01
Digits Only
4354763201
Product NDC
43547-632
Description
100 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (43547-632-01)
Marketing
Marketing Status
Brand
pemetrexed
Generic
pemetrexed
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b2088b2f-1c23-4bbf-91b3-1fc879180b8f", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728077"], "spl_set_id": ["bd0ada98-3237-4465-8ba2-3a12c33116fb"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (43547-632-01)", "package_ndc": "43547-632-01", "marketing_start_date": "20240701"}], "brand_name": "Pemetrexed", "product_id": "43547-632_b2088b2f-1c23-4bbf-91b3-1fc879180b8f", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "43547-632", "generic_name": "Pemetrexed", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/1"}], "application_number": "ANDA216582", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20271231"}