NDC 72338-101
Pemetrexed
Pemetrexed Disodium
Pemetrexed is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Waverley Pharma Inc. The primary component is Pemetrexed Disodium Heptahydrate.
| Product ID | 72338-101_6e125b95-8e00-4113-b710-247a4ad27da4 |
| NDC | 72338-101 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Pemetrexed |
| Generic Name | Pemetrexed Disodium |
| Dosage Form | Injection, Powder, Lyophilized, For Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2018-06-04 |
| Marketing Category | ANDA / |
| Application Number | ANDA211899 |
| Labeler Name | Waverley Pharma Inc |
| Substance Name | PEMETREXED DISODIUM HEPTAHYDRATE |
| Active Ingredient Strength | 500 mg/20mL |
| Pharm Classes | Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |