Package 70771-1693-1

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 70771-1693-1
Digits Only 7077116931
Product NDC 70771-1693
Description

1 VIAL in 1 CARTON (70771-1693-1) / 40 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2022-05-26
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": "fc5f4aa1-92c4-444b-8e64-53708c9a67bc", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["1728072", "1728077", "2601728"], "spl_set_id": ["6986de29-b077-48ac-ad2b-0cc478f72d89"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70771-1693-1)  / 40 mL in 1 VIAL", "package_ndc": "70771-1693-1", "marketing_start_date": "20220526"}], "brand_name": "pemetrexed", "product_id": "70771-1693_fc5f4aa1-92c4-444b-8e64-53708c9a67bc", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "70771-1693", "generic_name": "pemetrexed disodium", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "1000 mg/40mL"}], "application_number": "ANDA214073", "marketing_category": "ANDA", "marketing_start_date": "20220526", "listing_expiration_date": "20261231"}