Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 70069-0025-10 recalled?

Dexamethasone Sodium Phosphate · 10 VIAL in 1 CARTON (70069-025-10) / 10 mL in 1 VIAL

Yes — this exact package was recalled

1 FDA recall names the code 70069-0025-10 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

1 of these recalls is still ongoing.

Active ingredient
Dexamethasone Sodium Phosphate
Strength
DEXAMETHASONE SODIUM PHOSPHATE 10 mg/mL
Form
Injection, Solution · Intramuscular, Intravenous
Labeler
Somerset Therapeutics, LLC
Type
Human Prescription Drug
Product code
70069-0025

Recalls naming this package

Class II · Moderate risk

Dexamethasone Sodium Phosphate Injection

Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP impurity G (Impurity RU 49336) and dexamethasone formate.

Ongoing Impurity / degradation Somerset Therapeutics LLC D-0398-2026

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler