pemetrexed
Generic: pemetrexed disodium
Labeler: apotex corpDrug Facts
Product Profile
Brand Name
pemetrexed
Generic Name
pemetrexed disodium
Labeler
apotex corp
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
pemetrexed disodium 750 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
60505-6068
Product ID
60505-6068_bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209851
Marketing Start
2022-05-25
Marketing End
2026-06-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
605056068
Hyphenated Format
60505-6068
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 disodium (source: ndc)
Application Number
ANDA209851 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 750 mg/30mL
Packaging
- 1 VIAL in 1 CARTON (60505-6068-0) / 30 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": "bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30", "openfda": {"unii": ["2PKU919BA9"], "rxcui": ["2602136"], "spl_set_id": ["2e86f231-e0c7-2d43-2920-6c42d2469d11"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (60505-6068-0) / 30 mL in 1 VIAL", "package_ndc": "60505-6068-0", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}], "brand_name": "Pemetrexed", "product_id": "60505-6068_bcc07a71-41ab-e25e-aaf6-79bd6a7d5f30", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "60505-6068", "generic_name": "Pemetrexed disodium", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pemetrexed", "active_ingredients": [{"name": "PEMETREXED DISODIUM", "strength": "750 mg/30mL"}], "application_number": "ANDA209851", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20220525"}