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] |