United States · FDA National Drug Code directory
PREXXARTAN
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
- 76281-155_508c61d6-dbb1-5d06-e063-6394a90aa5ec
- Product NDC
- 76281-155
- Form
- SOLUTION
- Composition / generic term
- PREXXARTAN
- Labeler
- AptaPharma Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20260505
- Source listing expiry
- 20271231
Source-listed ingredients
- VALSARTAN — 4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 mL in 1 CUP, UNIT-DOSE (76281-155-56) · 76281-155-56
- 120 mL in 1 BOTTLE (76281-155-64) · 76281-155-64
- 473 mL in 1 BOTTLE (76281-155-82) · 76281-155-82
- 10 CUP, UNIT-DOSE in 1 TRAY (76281-155-99) / 20 mL in 1 CUP, UNIT-DOSE (76281-155-56) · 76281-155-99
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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