NDC 68001-544
Pemetrexed
Pemetrexed Disodium
Pemetrexed is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Bluepoint Laboratories. The primary component is Pemetrexed Disodium.
| Product ID | 68001-544_e65baa7b-24cf-5906-e053-2a95a90accd4 |
| NDC | 68001-544 |
| 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 | 2022-09-01 |
| Marketing Category | ANDA / |
| Application Number | ANDA203774 |
| Labeler Name | BluePoint Laboratories |
| Substance Name | PEMETREXED DISODIUM |
| 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 |