Details for New Drug Application (NDA): 211899
NDA 211899 describes PEMETREXED DISODIUM, which is a drug marketed by Accord Hlthcare, Amneal, Apotex, Baxter Hlthcare Corp, Biocon Pharma, Dr Reddys, Eugia Pharma, Fresenius Kabi Usa, Hetero Labs Ltd Vi, Hospira, Jiangsu Hansoh Pharm, Meitheal, Nang Kuang Pharm Co, Pharmobedient, Prinston Inc, Qilu Pharm Hainan, Somerset Theraps Llc, Zydus Pharms, and Sandoz, and is included in twenty-three NDAs. It is available from sixteen suppliers. Additional details are available on the PEMETREXED DISODIUM profile page.
The generic ingredient in PEMETREXED DISODIUM is pemetrexed disodium. There is one drug master file entry for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the pemetrexed disodium profile page.
The generic ingredient in PEMETREXED DISODIUM is pemetrexed disodium. There is one drug master file entry for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the pemetrexed disodium profile page.
Summary for 211899
| Tradename: | PEMETREXED DISODIUM |
| Applicant: | Somerset Theraps Llc |
| Ingredient: | pemetrexed disodium |
| Patents: | 0 |
Pharmacology for NDA: 211899
| Mechanism of Action | Folic Acid Metabolism Inhibitors |
Medical Subject Heading (MeSH) Categories for 211899
Suppliers and Packaging for NDA: 211899
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PEMETREXED DISODIUM | pemetrexed disodium | POWDER;INTRAVENOUS | 211899 | ANDA | Somerset Therapeutics LLC | 70069-834 | 70069-834-01 | 1 VIAL in 1 CARTON (70069-834-01) / 4 mL in 1 VIAL |
| PEMETREXED DISODIUM | pemetrexed disodium | POWDER;INTRAVENOUS | 211899 | ANDA | Somerset Therapeutics LLC | 70069-835 | 70069-835-01 | 1 VIAL in 1 CARTON (70069-835-01) / 20 mL in 1 VIAL |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | POWDER;INTRAVENOUS | Strength | EQ 100MG BASE/VIAL | ||||
| Approval Date: | May 25, 2022 | TE: | AP | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | POWDER;INTRAVENOUS | Strength | EQ 500MG BASE/VIAL | ||||
| Approval Date: | May 25, 2022 | TE: | AP | RLD: | No | ||||
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