pemetrexed

Generic: pemetrexed disodium

Labeler: zydus pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pemetrexed
Generic Name pemetrexed disodium
Labeler zydus pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pemetrexed disodium 1000 mg/40mL

Manufacturer
Zydus Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 70710-1674
Product ID 70710-1674_bf1de3fa-e7f8-4beb-beeb-6272709d13f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214073
Listing Expiration 2026-12-31
Marketing Start 2022-05-26

Pharmacologic Class

Classes
folate analog metabolic inhibitor [epc] folic acid metabolism inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707101674
Hyphenated Format 70710-1674

Supplemental Identifiers

RxCUI
1728072 1728077 2601728
UPC
0370710165512
UNII
2PKU919BA9

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name pemetrexed (source: ndc)
Generic Name pemetrexed disodium (source: ndc)
Application Number ANDA214073 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1000 mg/40mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (70710-1674-1) / 40 mL in 1 VIAL
source: ndc

Packages (1)

70710-1674-1 1 VIAL in 1 CARTON (70710-1674-1) / 40 mL in 1 VIAL

Ingredients (1)

pemetrexed disodium (1000 mg/40mL)

Linked Drug Pages (1)

pemetrexed ndc-match (0.9)

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"}