Pemetrexed

Generic: Pemetrexed disodium

Labeler: Ingenus Pharmaceuticals, LLC
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Pemetrexed
Generic Name Pemetrexed disodium
Labeler Ingenus Pharmaceuticals, LLC
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

PEMETREXED DISODIUM HEMIPENTAHYDRATE 100 mg/4mL

Identifiers & Regulatory

Product NDC 50742-340
Product ID 50742-340_58f8fad9-d6df-4916-ad09-36416553173a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204890
Marketing Start 2022-05-24
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742340
Hyphenated Format 50742-340

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 ANDA204890 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/4mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (50742-340-01) / 4 mL in 1 VIAL
source: ndc

Packages (1)

50742-340-01 1 VIAL in 1 CARTON (50742-340-01) / 4 mL in 1 VIAL

Ingredients (1)

PEMETREXED DISODIUM HEMIPENTAHYDRATE (100 mg/4mL)

Linked Drug Pages (1)

Pemetrexed ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "58f8fad9-d6df-4916-ad09-36416553173a", "openfda": {"unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["0346155f-a455-4044-8d5f-eacb97a8c8f0"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (50742-340-01)  / 4 mL in 1 VIAL", "package_ndc": "50742-340-01", "marketing_end_date": "20260228", "marketing_start_date": "20220524"}], "brand_name": "Pemetrexed", "product_id": "50742-340_58f8fad9-d6df-4916-ad09-36416553173a", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "50742-340", "generic_name": "Pemetrexed disodium", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/4mL"}], "application_number": "ANDA204890", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220524"}