| NDC Code | 0409-0040-10 |
|---|
| Package Description | 10 VIAL, MULTI-DOSE in 1 CARTON (0409-0040-10) / 5 mL in 1 VIAL, MULTI-DOSE (0409-0040-05) |
|---|
| Product NDC | 0409-0040 |
|---|
| 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 | 20221010 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074549 |
|---|
| Manufacturer | Hospira, Inc. |
|---|
| Substance Name | KETAMINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | General Anesthesia [PE], General Anesthetic [EPC] |
|---|
| DEA Schedule | CIII |
|---|