Class II · Moderate risk
Phenylephrine HCl Injection
Lack of Assurance of Sterility: customer complaints of loose crimped vial overseals which may result in a non-sterile product.
National Drug Code
Is NDC 25021-0315-01 recalled?
Phenylephrine Hydrochloride · 25 VIAL in 1 CARTON (25021-315-01) / 1 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 25021-0315-01 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
- Phenylephrine Hydrochloride
- Strength
- PHENYLEPHRINE HYDROCHLORIDE 10 mg/mL
- Form
- Injection, Solution · Intravenous
- Labeler
- Sagent Pharmaceuticals
- Type
- Human Prescription Drug
- Product code
- 25021-0315
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
- 25021-0163 See recall 2
- 25021-0254 Docetaxel 2
- 25021-0701 Ketorolac Tromethamine 2
- 25021-0113 See recall 1
- 25021-0139 See recall 1
- 25021-0140 See recall 1
Free recall alerts
Know the day your medication is recalled
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