Class II · Moderate risk
Hydromorphone
Lack of sterility assurance
National Drug Code
Is NDC 0703-0018-01 recalled?
Hydromorphone Hydrochloride · 1 VIAL in 1 CARTON (0703-0018-01) / 50 mL in 1 VIAL
Yes — this exact package was recalled
2 FDA recalls name the code 0703-0018-01 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
- Hydromorphone Hydrochloride
- Strength
- HYDROMORPHONE HYDROCHLORIDE 10 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous, Subcutaneous
- Labeler
- Teva Parenteral Medicines, Inc.
- Type
- Human Prescription Drug · DEA CII
- Product code
- 0703-0018
Recalls naming this package
Class II · Moderate risk
Hydromorphone Hydrochloride Injection
Presence of Particulate Matter: Silicone oil
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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