Pemetrexed 68001-0535
Product NDC
68001-0535- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 4, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA214632
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Pemetrexed Disodium Hemipentahydrate | 100 mg/4mL |
Drug Class
Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]
Packaging Options(1)
1 VIAL in 1 CARTON (68001-535-41) / 4 mL in 1 VIAL