Pemetrexed
- Product NDC
- 68001-551
- 11-digit product format
- 680010551
- Labeler code
- 68001
- Product ID
- 68001-551_e801f40f-0855-e83f-e053-2a95a90aaed8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pemetrexed disodium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- NDA214408
- Marketing category
- NDA
- Marketing start
- 2022-09-07
- Marketing end
- 0000-00-00
- Substance
- PEMETREXED DISODIUM HEMIPENTAHYDRATE
- Active strength
- 500 mg/20mL
- Pharmacologic classes
- Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-551-41 | 68001055141 | 1 VIAL in 1 CARTON (68001-551-41) > 20 mL in 1 VIAL | 1 vial | 2022-09-07 | 0000-00-00 | No | No | Current |