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  • Pemetrexed PEMETREXED DISODIUM 100 mg/4mL Zydus Lifesciences Limited
FDA Drug information

Pemetrexed

Read time: 1 mins
Marketing start date: 18 Nov 2024
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Summary of product characteristics


Effective Time

20220526

Version

1

Spl Product Data Elements

pemetrexed pemetrexed disodium PEMETREXED DISODIUM PEMETREXED MANNITOL HYDROCHLORIC ACID SODIUM HYDROXIDE pemetrexed pemetrexed disodium PEMETREXED DISODIUM PEMETREXED MANNITOL HYDROCHLORIC ACID SODIUM HYDROXIDE pemetrexed pemetrexed disodium PEMETREXED DISODIUM PEMETREXED MANNITOL HYDROCHLORIC ACID SODIUM HYDROXIDE

Application Number

ANDA214073

Brand Name

Pemetrexed

Generic Name

pemetrexed disodium

Product Ndc

70771-1691

Product Type

HUMAN PRESCRIPTION DRUG

Route

INTRAVENOUS

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1691-1 Pemetrexed for Injection, USP 100 mg/vial For intravenous use only. Single-Dose Vial Rx only NDC 70771-1691-1 Pemetrexed for Injection, USP 100 mg/vial For intravenous use only. One Single-Dose Vial Carton Rx only NDC 70771-1692-1 Pemetrexed for Injection, USP 500 mg/vial For intravenous use only. Single-Dose Vial Rx only NDC 70771-1692-1 Pemetrexed for Injection, USP 500 mg/vial For intravenous use only. One Single-Dose Vial Carton Rx only NDC 70771-1693-1 Pemetrexed for Injection, USP 1000 mg/vial For intravenous use only. Single-Dose Vial Rx only NDC 70771-1693-1 Pemetrexed for Injection, USP 1000 mg/vial For intravenous use only. One Single-Dose Vial Carton Rx only 100 mg vial label 100 mg carton label 500 mg vial label 500 mg carton label 1,000 mg vial label 1,000 mg carton label

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Drugs appearing in this section are approved by the FDA. For regions outside of the United States, this content is for informational purposes only and may not be aligned with local regulatory approvals or guidance.