Package 71288-166-91
Brand: pemetrexed
Generic: pemetrexed disodiumPackage Facts
Identity
Package NDC
71288-166-91
Digits Only
7128816691
Product NDC
71288-166
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (71288-166-91) / 10 mL in 1 VIAL, SINGLE-DOSE
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": "b38927c4-2b38-4d5c-be9f-86ba95ddc038", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["e0d000a3-b9d2-4fa9-9591-f7acb077481d"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-166-91) / 10 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-166-91", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "71288-166_b38927c4-2b38-4d5c-be9f-86ba95ddc038", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "71288-166", "generic_name": "Pemetrexed disodium", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/10mL"}], "application_number": "ANDA208696", "marketing_category": "ANDA", "marketing_start_date": "20220525", "listing_expiration_date": "20261231"}