Class II ยท Moderate risk
Vasostrict
Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.
National Drug Code
Is NDC 42023-0237-10 recalled?
Vasostrict · 10 VIAL in 1 CARTON (42023-237-10) / 100 mL in 1 VIAL (42023-237-01)
Yes — this exact package was recalled
1 FDA recall names the code 42023-0237-10 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.
1 of these recalls is still ongoing.
- Active ingredient
- Vasopressin
- Strength
- VASOPRESSIN, UNSPECIFIED .2 [USP'U]/mL
- Form
- Injection · Intravenous
- Labeler
- Par Health USA, LLC
- Type
- Human Prescription Drug
- Product code
- 42023-0237
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
- 42023-0179 Buprenorphine Hydrochloride 4
- 42023-0103 See recall 1
- 42023-0116 Pitocin 1
- 42023-0159 Adrenalin 1
- 42023-0168 Adrenalin 1
- 42023-0206 See recall 1
Free recall alerts
Know the day your medication is recalled
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