United States · FDA National Drug Code directory
Trazimera
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
- 0069-0308_6bb3d11b-6f9e-408c-a957-b7bacaf9e175
- Product NDC
- 0069-0308
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- trastuzumab-qyyp
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Marketing category
- BLA
- Marketing start / end (source format)
- 20210310
- Source listing expiry
- 20271231
Source-listed ingredients
- TRASTUZUMAB — 150 mg/7.15mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (0069-0308-01) / 7.15 mL in 1 VIAL · 0069-0308-01
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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