FDA
Pemetrexed Disodium
The FDA lists this product in 54 strengths and forms.
Composition
- Active ingredients
- PEMETREXED DISODIUM EQ 500MG BASE/VIAL
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- PEMETREXED DISODIUM EQ 1GM BASE/VIAL · PowderANDA211090-001 · Discontinued
- PEMETREXED DISODIUM EQ 1GM BASE/40ML (EQ 25MG BASE/ML) · SolutionNDA214218-003 · Prescription
- PEMETREXED DISODIUM EQ 100MG BASE/4ML (EQ 25MG BASE/ML) · SolutionNDA214218-001 · Prescription
- PEMETREXED DISODIUM EQ 500MG BASE/20ML (EQ 25MG BASE/ML) · SolutionNDA214218-002 · Prescription
- PEMETREXED DISODIUM EQ 100MG BASE/VIAL · PowderANDA216582-001 · Prescription
- PEMETREXED DISODIUM EQ 1GM BASE/VIAL · PowderANDA203485-003 · Prescription
- PEMETREXED DISODIUM EQ 100MG BASE/VIAL · PowderANDA203485-001 · Prescription
- PEMETREXED DISODIUM EQ 500MG BASE/VIAL · PowderANDA203485-002 · Prescription
- PEMETREXED DISODIUM EQ 500MG BASE/VIAL · PowderANDA203774-002 · Prescription
- PEMETREXED DISODIUM EQ 100MG BASE/VIAL · PowderANDA203774-001 · Prescription
- PEMETREXED DISODIUM EQ 750MG BASE/VIAL · Powder
At a glance
- Brand name
- Pemetrexed Disodium
- Route
- Intravenous
- Dosage form
- Powder
- Applicant
- Fresenius Kabi USA
- Status
- Prescription
- FDA approval
- 25 May 2022
- Application
- ANDA090384-002