Product NDC: | 0781-1436 |
Proprietary Name: | Fluphenazine Hydrochloride |
Non Proprietary Name: | Fluphenazine Hydrochloride |
Active Ingredient(s): | 1 mg/1 & nbsp; Fluphenazine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-1436 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089583 |
Marketing Category: | ANDA |
Start Marketing Date: | 19871016 |
Package NDC: | 0781-1436-13 |
Package Description: | 10 BLISTER PACK in 1 CARTON (0781-1436-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Code | 0781-1436-13 |
Proprietary Name | Fluphenazine Hydrochloride |
Package Description | 10 BLISTER PACK in 1 CARTON (0781-1436-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
Product NDC | 0781-1436 |
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 | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |