Product NDC: | 52959-940 |
Proprietary Name: | Perphenazine |
Non Proprietary Name: | perphenazine |
Active Ingredient(s): | 8 mg/1 & nbsp; perphenazine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, SUGAR COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52959-940 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040226 |
Marketing Category: | ANDA |
Start Marketing Date: | 19981231 |
Package NDC: | 52959-940-60 |
Package Description: | 60 TABLET, SUGAR COATED in 1 BOTTLE, PLASTIC (52959-940-60) |
NDC Code | 52959-940-60 |
Proprietary Name | Perphenazine |
Package Description | 60 TABLET, SUGAR COATED in 1 BOTTLE, PLASTIC (52959-940-60) |
Product NDC | 52959-940 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | perphenazine |
Dosage Form Name | TABLET, SUGAR COATED |
Route Name | ORAL |
Start Marketing Date | 19981231 |
Marketing Category Name | ANDA |
Labeler Name | H.J. Harkins Company, Inc. |
Substance Name | PERPHENAZINE |
Strength Number | 8 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |