NDC 23155-893
Methohexital Sodium 500 mg per 500 mg injection
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. names for other drugs.
Recalls
- Jun 7, 2026 · Class II · Onesource Specialty Pharma Limited
Failed Impurities/Degradation Specifications
Lots: Lot #: 7000612A, Exp. Date 1/2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methohexital: every company that makes it
- Form
- injection, intramuscular; intravenous; rectal
- Strength
- 500 mg per 500 mg
- Approval
- ANDA ANDA215488
- On the market since
- Dec 12, 2024
- Package NDCs
23155-893-31- Official label
- DailyMed (National Library of Medicine), updated Jul 27, 2026
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