| NDC Code | 52584-040-05 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 BAG (52584-040-05) > 5 mL in 1 VIAL, MULTI-DOSE |
|---|
| Product NDC | 52584-040 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ketamine Hydrochloride |
|---|
| Non-Proprietary Name | Ketamine Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20121016 |
|---|
| End Marketing Date | 20230801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074549 |
|---|
| Manufacturer | General Injectables & Vaccines, Inc |
|---|
| Substance Name | KETAMINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | General Anesthesia [PE], General Anesthetic [EPC] |
|---|
| DEA Schedule | CIII |
|---|