Pemetrexed
- Product NDC
- 70860-203
- 11-digit product format
- 708600203
- Labeler code
- 70860
- Product ID
- 70860-203_875662c9-067b-457d-907d-bc22851a8607
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- pemetrexed disodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA207352
- Marketing category
- ANDA
- Marketing start
- 2022-05-25
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-203-50 | 70860020350 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70860-203-50) > 20 mL in 1 VIAL, SINGLE-DOSE | 2022-05-25 | 0000-00-00 | No | No | Current |