| NDC Code | 0641-1397-35 |
|---|
| Package Description | 25 AMPULE in 1 CARTON (0641-1397-35) / 1 mL in 1 AMPULE (0641-1397-31) |
|---|
| Product NDC | 0641-1397 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Non-Proprietary Name | Chlorpromazine Hydrochloride |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR |
|---|
| Start Marketing Date | 19740725 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA083329 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | CHLORPROMAZINE HYDROCHLORIDE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
|---|