KETAMINE HYDROCHLORIDE
- Product NDC
- 52584-038
- 11-digit product format
- 525840038
- Labeler code
- 52584
- Product ID
- 52584-038_8dd340cd-7bce-4ab7-9a66-2d6653b4fcf3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ketamine hydrochloride
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA074549
- Marketing category
- ANDA
- Marketing start
- 2012-10-11
- Marketing end
- 0000-00-00
- Substance
- KETAMINE HYDROCHLORIDE
- Active strength
- 50 mg/mL
- Pharmacologic classes
- General Anesthesia [PE],General Anesthetic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-038-10 | 52584003810 | 1 VIAL in 1 BAG (52584-038-10) > 10 mL in 1 VIAL | 1 vial | 2012-10-11 | 0000-00-00 | No | No | Current |