pemrydi rtu
Generic: pemetrexed disodium
Labeler: amneal pharmaceuticals llcDrug Facts
Product Profile
Brand Name
pemrydi rtu
Generic Name
pemetrexed disodium
Labeler
amneal pharmaceuticals llc
Dosage Form
INJECTION
Routes
Active Ingredients
pemetrexed disodium hemipentahydrate 100 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
70121-2453
Product ID
70121-2453_b6a00be1-95d1-4b91-93bf-4430a57eeff6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA215179
Listing Expiration
2026-12-31
Marketing Start
2023-06-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
701212453
Hyphenated Format
70121-2453
Supplemental Identifiers
RxCUI
UPC
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
pemrydi rtu (source: ndc)
Generic Name
pemetrexed disodium (source: ndc)
Application Number
NDA215179 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/10mL
Packaging
- 1 VIAL in 1 CARTON (70121-2453-1) / 10 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": "b6a00be1-95d1-4b91-93bf-4430a57eeff6", "openfda": {"upc": ["0370121246213", "0370121246114", "0370121245315"], "unii": ["F4GSH45R4C"], "rxcui": ["2637958", "2637964", "2637966", "2637967", "2637968", "2637969"], "spl_set_id": ["0f006b06-ab85-423d-ba0c-dfc3fc25844e"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70121-2453-1) / 10 mL in 1 VIAL", "package_ndc": "70121-2453-1", "marketing_start_date": "20230606"}], "brand_name": "PEMRYDI RTU", "product_id": "70121-2453_b6a00be1-95d1-4b91-93bf-4430a57eeff6", "dosage_form": "INJECTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "70121-2453", "generic_name": "Pemetrexed disodium", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PEMRYDI RTU", "active_ingredients": [{"name": "PEMETREXED DISODIUM HEMIPENTAHYDRATE", "strength": "100 mg/10mL"}], "application_number": "NDA215179", "marketing_category": "NDA", "marketing_start_date": "20230606", "listing_expiration_date": "20261231"}