Class II · Moderate risk
Haloperidol Decanoate Injection 50mg/mL
Lack of Assurance of Sterility: Media fill with bacterial contamination
National Drug Code
Is NDC 70069-0381-01 recalled?
Haloperidol Decanoate · 1 VIAL, SINGLE-DOSE in 1 CARTON (70069-381-01) / 1 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
2 FDA recalls name the code 70069-0381-01 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.
2 of these recalls are still ongoing.
- Active ingredient
- Haloperidol Decanoate
- Strength
- HALOPERIDOL DECANOATE 50 mg/mL
- Form
- Injection · Intramuscular
- Labeler
- Somerset Therapeutics, LLC
- Type
- Human Prescription Drug
- Product code
- 70069-0381
Recalls naming this package
Class II · Moderate risk
Haloperidol decanoate Injection 50mg/mL
Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
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
- 70069-0025 Dexamethasone Sodium Phosphate 1
- 70069-0101 Methocarbamol 1
- 70069-0141 Cisatracurium Besylate 1
- 70069-0151 Cisatracurium Besylate 1
- 70069-0161 Cisatracurium Besylate 1
- 70069-0231 Brimonidine Tartrate 1
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