Class II · Moderate risk
Progesterone Injection USP
Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.
National Drug Code
Is NDC 55150-0306-10 recalled?
Progesterone · 10 mL in 1 VIAL, MULTI-DOSE (55150-306-10)
Yes — this exact package was recalled
2 FDA recalls name the code 55150-0306-10 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.
2 of these recalls are still ongoing.
- Active ingredient
- Progesterone
- Strength
- PROGESTERONE 50 mg/mL
- Form
- Injection, Solution · Intramuscular
- Labeler
- Eugia US LLC
- Type
- Human Prescription Drug
- Product code
- 55150-0306
Recalls naming this package
Class II · Moderate risk
Progesterone Injection
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
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
- 55150-0120 Piperacillin and Tazobactam 2
- 55150-0183 Nicardipine Hydrochloride 2
- 55150-0202 Pantoprazole Sodium 2
- 55150-0242 Linezolid 2
- 55150-0243 Levofloxacin 2
- 55150-0113 Ampicillin 1
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