| Product NDC: | 55390-465 |
| Proprietary Name: | Fluphenazine Decanoate |
| Non Proprietary Name: | Fluphenazine Decanoate |
| Active Ingredient(s): | 25 mg/mL & nbsp; Fluphenazine Decanoate |
| Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55390-465 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074531 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960830 |
| Package NDC: | 55390-465-05 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 BOX (55390-465-05) > 5 mL in 1 VIAL, MULTI-DOSE |
| NDC Code | 55390-465-05 |
| Proprietary Name | Fluphenazine Decanoate |
| Package Description | 1 VIAL, MULTI-DOSE in 1 BOX (55390-465-05) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 55390-465 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluphenazine Decanoate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 19960830 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | FLUPHENAZINE DECANOATE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |