Product NDC: | 49349-189 |
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) |
Product NDC: | 49349-189 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA089804 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101223 |
Package NDC: | 49349-189-24 |
Package Description: | 200 TABLET, FILM COATED in 1 CANISTER (49349-189-24) |
NDC Code | 49349-189-24 |
Proprietary Name | FLUPHENAZINE HYDROCHLORIDE |
Package Description | 200 TABLET, FILM COATED in 1 CANISTER (49349-189-24) |
Product NDC | 49349-189 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FLUPHENAZINE HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20101223 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | FLUPHENAZINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |