Ketamine Hydrochloride
- Product NDC
- 70518-2787
- 11-digit product format
- 705182787
- Labeler code
- 70518
- Product ID
- 70518-2787_d70ec608-8092-92db-e053-2995a90af2d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketamine Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076092
- Marketing category
- ANDA
- Marketing start
- 2020-06-16
- Marketing end
- 0000-00-00
- Substance
- KETAMINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- General Anesthesia [PE], General Anesthetic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2787-0 | 70518278700 | 10 VIAL in 1 CARTON (70518-2787-0) > 20 mL in 1 VIAL (70518-2787-1) | 10 vial | 2020-06-16 | 0000-00-00 | No | No | Current |