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Fluphenazine Hydrochloride
Fluphenazine Hydrochloride - 0781-1439-13 - (Fluphenazine Hydrochloride)
Drug Information of Fluphenazine Hydrochloride
| Product NDC: | 0781-1439 |
| Proprietary Name: | Fluphenazine Hydrochloride |
| Non Proprietary Name: | Fluphenazine Hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; Fluphenazine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluphenazine Hydrochloride
| Product NDC: | 0781-1439 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089586 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19871016 |
Package Information of Fluphenazine Hydrochloride
| Package NDC: | 0781-1439-13 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (0781-1439-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Fluphenazine Hydrochloride
| NDC Code | 0781-1439-13 |
| Proprietary Name | Fluphenazine Hydrochloride |
| Package Description | 10 BLISTER PACK in 1 CARTON (0781-1439-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0781-1439 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluphenazine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19871016 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
