National Drug Code
Is NDC 42023-0105-01 recalled?
Brevital Sodium · 1 VIAL in 1 CARTON (42023-105-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Recall announced for this product
announced by the firm and posted by FDA; not yet in FDA’s classified recall data
-
Brevital Sodium 500 mg/vial for Injection
· Par Health ·
Reason Presence of particulate matter identified as cellulose
- Active ingredient
- methohexital sodium
- Strength
- METHOHEXITAL SODIUM 500 mg/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intramuscular, Intravenous, Rectal
- Labeler
- Par Health USA, LLC
- Type
- Human Prescription Drug · DEA CIV
- Product code
- 42023-0105
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
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