Package 70069-834-01
Brand: pemetrexed
Generic: pemetrexed disodiumPackage Facts
Identity
Package NDC
70069-834-01
Digits Only
7006983401
Product NDC
70069-834
Description
1 VIAL in 1 CARTON (70069-834-01) / 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": "34c64c32-89bd-e0a0-e063-6394a90a8ddf", "openfda": {"unii": ["9T47E4OM16"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["39219e4b-80a6-4d4f-96a3-1202e542d050"], "manufacturer_name": ["Somerset Therapeutics LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70069-834-01) / 4 mL in 1 VIAL", "package_ndc": "70069-834-01", "marketing_start_date": "20250415"}], "brand_name": "Pemetrexed", "product_id": "70069-834_34c64c32-89bd-e0a0-e063-6394a90a8ddf", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "70069-834", "generic_name": "Pemetrexed disodium", "labeler_name": "Somerset Therapeutics LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEPTAHYDRATE", "strength": "100 mg/4mL"}], "application_number": "ANDA211899", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}