Class I · High risk
Hydromorphone
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
National Drug Code
Is NDC 0703-0110-03 recalled?
Hydromorphone Hydrochloride · 10 VIAL in 1 CARTON (0703-0110-03) / 1 mL in 1 VIAL (0703-0110-01)
Yes — this exact package was recalled
1 FDA recall names the code 0703-0110-03 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
- 0703-0110
Recalls naming this package
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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