pemetrexed

Generic: pemetrexed disodium

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

pemetrexed disodium hemipentahydrate 100 mg/4mL

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-336
Product ID 31722-336_31b2e68a-5c70-b490-e063-6294a90aaab0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215460
Listing Expiration 2026-12-31
Marketing Start 2024-06-14

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 31722336
Hyphenated Format 31722-336

Supplemental Identifiers

RxCUI
1728072 1728077
UPC
0331722337311 0331722336314
UNII
F4GSH45R4C

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 ANDA215460 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/4mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (31722-336-31) / 4 mL in 1 VIAL
source: ndc

Packages (1)

31722-336-31 1 VIAL in 1 CARTON (31722-336-31) / 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": "31b2e68a-5c70-b490-e063-6294a90aaab0", "openfda": {"upc": ["0331722337311", "0331722336314"], "unii": ["F4GSH45R4C"], "rxcui": ["1728072", "1728077"], "spl_set_id": ["2ca1ce75-5284-4282-b76a-3700d203c714"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (31722-336-31)  / 4 mL in 1 VIAL", "package_ndc": "31722-336-31", "marketing_start_date": "20240614"}], "brand_name": "Pemetrexed", "product_id": "31722-336_31b2e68a-5c70-b490-e063-6294a90aaab0", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "31722-336", "generic_name": "Pemetrexed disodium", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/4mL"}], "application_number": "ANDA215460", "marketing_category": "ANDA", "marketing_start_date": "20240614", "listing_expiration_date": "20261231"}