Pemetrexed
- Product NDC
- 60505-6067
- 11-digit product format
- 605056067
- Labeler code
- 60505
- Product ID
- 60505-6067_77cfaf5f-90c7-60f7-61a7-f5d03bdce244
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pemetrexed disodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Apotex Corp
- Application
- ANDA209085
- Marketing category
- ANDA
- Marketing start
- 2022-05-25
- Marketing end
- 0000-00-00
- Substance
- PEMETREXED DISODIUM
- Active strength
- 1000 mg/40mL
- 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 |
|---|
| 60505-6067-0 | 60505606700 | 1 VIAL in 1 CARTON (60505-6067-0) > 40 mL in 1 VIAL | 1 vial | 2022-05-25 | 0000-00-00 | No | No | Current |