Class II · Moderate risk
Hydromorphone
Lack of sterility assurance
National Drug Code
Is NDC 0409-2634-50 recalled?
Hydromorphone Hydrochloride · 1 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-50) / 50 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
2 FDA recalls name the code 0409-2634-50 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
- Hydromorphone Hydrochloride
- Strength
- HYDROMORPHONE HYDROCHLORIDE 10 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Hospira, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0409-2634
Recalls naming this package
Class I · High risk
Hydromorphone
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Class II · Moderate risk
Hydromorphone Hydrochloride Injection
Presence of Particulate Matter: Silicone oil
Class II · Moderate risk
Hydromorphone Hydrochloride Injection
Lack Of Assurance Of Sterility: Confirmed customer complaints of glass product container vials that may be broken or cracked.
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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