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Fluphenazine Hydrochloride
Fluphenazine Hydrochloride - 63323-281-10 - (FLUPHENAZINE HYDROCHLORIDE)
Drug Information of Fluphenazine Hydrochloride
| Product NDC: | 63323-281 |
| Proprietary Name: | Fluphenazine Hydrochloride |
| Non Proprietary Name: | FLUPHENAZINE HYDROCHLORIDE |
| Active Ingredient(s): | 2.5 mg/mL & nbsp; FLUPHENAZINE HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluphenazine Hydrochloride
| Product NDC: | 63323-281 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089556 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101228 |
Package Information of Fluphenazine Hydrochloride
| Package NDC: | 63323-281-10 |
| Package Description: | 1 VIAL in 1 BOX (63323-281-10) > 10 mL in 1 VIAL |
NDC Information of Fluphenazine Hydrochloride
| NDC Code | 63323-281-10 |
| Proprietary Name | Fluphenazine Hydrochloride |
| Package Description | 1 VIAL in 1 BOX (63323-281-10) > 10 mL in 1 VIAL |
| Product NDC | 63323-281 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUPHENAZINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR |
| Start Marketing Date | 20101228 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
