Class III · Low risk
Cisatracurium Besylate Injection USP
Subpotent product:out of specification assay results observed during long term stability testing.
National Drug Code
Is NDC 70069-0161-01 recalled?
Cisatracurium Besylate · 1 VIAL in 1 CARTON (70069-161-01) / 10 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 70069-0161-01 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.
1 of these recalls is still ongoing.
- Active ingredient
- Cisatracurium Besylate
- Strength
- CISATRACURIUM BESYLATE 2 mg/mL
- Form
- Injection · Intravenous
- Labeler
- Somerset Therapeutics, LLC
- Type
- Human Prescription Drug
- Product code
- 70069-0161
Recalls naming this package
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
- 70069-0381 Haloperidol Decanoate 2
- 70069-0025 Dexamethasone Sodium Phosphate 1
- 70069-0101 Methocarbamol 1
- 70069-0141 Cisatracurium Besylate 1
- 70069-0151 Cisatracurium Besylate 1
- 70069-0231 Brimonidine Tartrate 1
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