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Fluphenazine Decanoate
Fluphenazine Decanoate - 63323-272-05 - (FLUPHENAZINE DECANOATE)
Drug Information of Fluphenazine Decanoate
| Product NDC: | 63323-272 |
| 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, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluphenazine Decanoate
| Product NDC: | 63323-272 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071413 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101215 |
Package Information of Fluphenazine Decanoate
| Package NDC: | 63323-272-05 |
| Package Description: | 1 VIAL in 1 CARTON (63323-272-05) > 5 mL in 1 VIAL |
NDC Information of Fluphenazine Decanoate
| NDC Code | 63323-272-05 |
| Proprietary Name | Fluphenazine Decanoate |
| Package Description | 1 VIAL in 1 CARTON (63323-272-05) > 5 mL in 1 VIAL |
| Product NDC | 63323-272 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUPHENAZINE DECANOATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 20101215 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | FLUPHENAZINE DECANOATE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
