| NDC Code | 55390-077-01 |
|---|
| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (55390-077-01) > 10 mL in 1 VIAL |
|---|
| Product NDC | 55390-077 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Prochlorperazine Edisylate |
|---|
| Non-Proprietary Name | Prochlorperazine Edisylate |
|---|
| Dosage Form | INJECTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20040726 |
|---|
| End Marketing Date | 20150331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040540 |
|---|
| Manufacturer | Bedford Laboratories |
|---|
| Substance Name | PROCHLORPERAZINE EDISYLATE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
|---|