pemetrexed
Generic: pemetrexed
Labeler: teva pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
pemetrexed
Generic Name
pemetrexed
Labeler
teva pharmaceuticals, inc.
Dosage Form
SOLUTION, CONCENTRATE
Routes
Active Ingredients
pemetrexed monohydrate 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0480-4516
Product ID
0480-4516_21155bd2-118e-4ce6-adb8-dddc69ae34c7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA208419
Listing Expiration
2026-12-31
Marketing Start
2022-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04804516
Hyphenated Format
0480-4516
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
pemetrexed (source: ndc)
Generic Name
pemetrexed (source: ndc)
Application Number
NDA208419 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (0480-4516-01) / 4 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "21155bd2-118e-4ce6-adb8-dddc69ae34c7", "openfda": {"unii": ["236Y2F7D9J"], "rxcui": ["2602363", "2602365", "2602366"], "spl_set_id": ["8b660f68-b770-4e0a-b2f9-25e663deecc3"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0480-4516-01) / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0480-4516-01", "marketing_start_date": "20220601"}], "brand_name": "Pemetrexed", "product_id": "0480-4516_21155bd2-118e-4ce6-adb8-dddc69ae34c7", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0480-4516", "generic_name": "Pemetrexed", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED MONOHYDRATE", "strength": "25 mg/mL"}], "application_number": "NDA208419", "marketing_category": "NDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}