| NDC Code | 0641-1496-35 |
|---|
| Package Description | 25 AMPULE in 1 PACKAGE (0641-1496-35) / 1 mL in 1 AMPULE (0641-1496-31) |
|---|
| Product NDC | 0641-1496 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Promethazine Hydrochloride |
|---|
| Non-Proprietary Name | Promethazine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR |
|---|
| Start Marketing Date | 19730919 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA083312 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | PROMETHAZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|