Ketamine Hydrochloride
- Product NDC
- 71872-7258
- 11-digit product format
- 718727258
- Labeler code
- 71872
- Product ID
- 71872-7258_fa5a5cb2-9f38-fbff-e053-6294a90a83a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketamine Hydrochloride
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA074524
- Marketing category
- ANDA
- Marketing start
- 1996-07-01
- Substance
- KETAMINE HYDROCHLORIDE
- Active strength
- 100 mg/mL
- Pharmacologic classes
- General Anesthesia [PE], General Anesthetic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| O18YUO0I83 | KETAMINE HYDROCHLORIDE | 1867-66-9 | KETAMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7258-1 | 71872725801 | 1 VIAL in 1 BAG (71872-7258-1) / 5 mL in 1 VIAL | 1 vial | 2021-07-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ketamine Hydrochloride | Medical Purchasing Solutions, LLC | 2023-04-27 | HUMAN PRESCRIPTION DRUG LABEL | 2 |