Package 31722-336-31
Brand: pemetrexed
Generic: pemetrexed disodiumPackage Facts
Identity
Package NDC
31722-336-31
Digits Only
3172233631
Product NDC
31722-336
Description
1 VIAL in 1 CARTON (31722-336-31) / 4 mL in 1 VIAL
Marketing
Marketing Status
Brand
pemetrexed
Generic
pemetrexed disodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "31b2e68a-5c70-b490-e063-6294a90aaab0", "openfda": {"upc": ["0331722337311", "0331722336314"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["2ca1ce75-5284-4282-b76a-3700d203c714"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (31722-336-31) / 4 mL in 1 VIAL", "package_ndc": "31722-336-31", "marketing_start_date": "20240614"}], "brand_name": "Pemetrexed", "product_id": "31722-336_31b2e68a-5c70-b490-e063-6294a90aaab0", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "31722-336", "generic_name": "Pemetrexed disodium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/4mL"}], "application_number": "ANDA215460", "marketing_category": "ANDA", "marketing_start_date": "20240614", "listing_expiration_date": "20261231"}