pemfexy
Generic: pemetrexed
Labeler: eagle pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
pemfexy
Generic Name
pemetrexed
Labeler
eagle pharmaceuticals, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
pemetrexed monohydrate 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42367-531
Product ID
42367-531_efadeccf-c754-46aa-999e-4da07a4cd2ce
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA209472
Marketing Start
2022-02-01
Marketing End
2028-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42367531
Hyphenated Format
42367-531
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
pemfexy (source: ndc)
Generic Name
pemetrexed (source: ndc)
Application Number
NDA209472 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 1 VIAL in 1 CARTON (42367-531-33) / 20 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "efadeccf-c754-46aa-999e-4da07a4cd2ce", "openfda": {"unii": ["236Y2F7D9J"], "rxcui": ["2590672", "2590677"], "spl_set_id": ["2308f4e8-21c8-49c1-a5b8-deb8610bac6a"], "manufacturer_name": ["Eagle Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42367-531-33) / 20 mL in 1 VIAL", "package_ndc": "42367-531-33", "marketing_end_date": "20280430", "marketing_start_date": "20220201"}], "brand_name": "Pemfexy", "product_id": "42367-531_efadeccf-c754-46aa-999e-4da07a4cd2ce", "dosage_form": "INJECTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "42367-531", "generic_name": "pemetrexed", "labeler_name": "Eagle Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemfexy", "active_ingredients": [{"name": "PEMETREXED MONOHYDRATE", "strength": "25 mg/mL"}], "application_number": "NDA209472", "marketing_category": "NDA", "marketing_end_date": "20280430", "marketing_start_date": "20220201"}