United States · FDA National Drug Code directory
pemetrexed
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70771-1693_fc5f4aa1-92c4-444b-8e64-53708c9a67bc
- Product NDC
- 70771-1693
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- pemetrexed disodium
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220526
- Source listing expiry
- 20261231
Source-listed ingredients
- PEMETREXED DISODIUM — 1000 mg/40mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (70771-1693-1) / 40 mL in 1 VIAL · 70771-1693-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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