pemetrexed

Generic: pemetrexed disodium

Labeler: somerset therapeutics llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pemetrexed
Generic Name pemetrexed disodium
Labeler somerset therapeutics llc
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

pemetrexed disodium heptahydrate 100 mg/4mL

Manufacturer
Somerset Therapeutics LLC

Identifiers & Regulatory

Product NDC 70069-834
Product ID 70069-834_34c64c32-89bd-e0a0-e063-6394a90a8ddf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211899
Listing Expiration 2026-12-31
Marketing Start 2025-04-15

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 70069834
Hyphenated Format 70069-834

Supplemental Identifiers

RxCUI
1728072 1728077
UNII
9T47E4OM16

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 ANDA211899 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/4mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (70069-834-01) / 4 mL in 1 VIAL
source: ndc

Packages (1)

70069-834-01 1 VIAL in 1 CARTON (70069-834-01) / 4 mL in 1 VIAL

Ingredients (1)

pemetrexed disodium heptahydrate (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": "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"}