Package 70710-1674-1

Brand: pemetrexed

Generic: pemetrexed disodium
NDC Package

Package Facts

Identity

Package NDC 70710-1674-1
Digits Only 7071016741
Product NDC 70710-1674
Description

1 VIAL in 1 CARTON (70710-1674-1) / 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": "bf1de3fa-e7f8-4beb-beeb-6272709d13f2", "openfda": {"upc": ["0370710165512"], "unii": ["2PKU919BA9"], "rxcui": ["1728072", "1728077", "2601728"], "spl_set_id": ["363665ca-db15-4123-84ac-0ae66b5f1363"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70710-1674-1)  / 40 mL in 1 VIAL", "package_ndc": "70710-1674-1", "marketing_start_date": "20220526"}], "brand_name": "pemetrexed", "product_id": "70710-1674_bf1de3fa-e7f8-4beb-beeb-6272709d13f2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "70710-1674", "generic_name": "pemetrexed disodium", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}