Class III · Low risk
Dexamethasone Sodium Phosphate Injection
Failed Impurities/Degradation Specifications: high out of specification results for Dexamethasone adduct (related compound).
National Drug Code
Is NDC 0641-6146-01 recalled?
Dexamethasone Sodium Phosphate
Yes — this exact package was recalled
1 FDA recall names the code 0641-6146-01 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.
- Active ingredient
- Dexamethasone Sodium Phosphate
- Strength
- DEXAMETHASONE SODIUM PHOSPHATE 4 mg/mL
- Form
- Injection · Intra-Articular, Intralesional, Intramuscular, Intravenous, Soft Tissue
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0641-6146
Recalls naming this package
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
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