United States · FDA National Drug Code directory
Dexamethasone Sodium Phosphate
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
- 70518-4372_5b0d63e4-763a-0346-e063-6394a90a0e74
- Product NDC
- 70518-4372
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dexamethasone Sodium Phosphate
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250625
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXAMETHASONE SODIUM PHOSPHATE — 4 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (70518-4372-0) / 1 mL in 1 VIAL (70518-4372-1) · 70518-4372-0
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →