Methohexital Sodium
NDC 23155-893, Methohexital Sodium, injection, from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
- Product NDC
- 23155-893
- Status
- Listed
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR, INTRAVENOUS, RECTAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215488
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/23155-893 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHOHEXITAL SODIUM500 mg/500mg
Pharmacologic classes
Barbiturate [EPC]; Barbiturates [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 23155-893-31 | 23155089331 | 1 VIAL in 1 CARTON (23155-893-31) / 500 mg in 1 VIAL |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/f76d4ab9-2f6c-420b-afec-b9cdfdc083ce
Use it
Look up 23155-893 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/23155-893 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 23155-893. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.