ketamine hydrochloride
NDC 65219-184, ketamine hydrochloride, injection, from Fresenius Kabi USA, LLC.
- Product NDC
- 65219-184
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215808
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/65219-184 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- KETAMINE HYDROCHLORIDE10 mg/mL
Pharmacologic classes
General Anesthesia [PE]; General Anesthetic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65219-184-20 | 65219018420 | 10 VIAL in 1 TRAY (65219-184-20) / 20 mL in 1 VIAL (65219-184-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cc67b0fd-ca73-49f6-b5ca-705dc7331776
Use it
Look up 65219-184 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65219-184 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65219-184. 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.