Product NDC: | 43353-788 |
Proprietary Name: | quetiapine fumarate |
Non Proprietary Name: | quetiapine fumarate |
Active Ingredient(s): | 25 mg/1 & nbsp; quetiapine fumarate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43353-788 |
Labeler Name: | Aphena Pharma Solutions - Tennessee, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090960 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120327 |
Package NDC: | 43353-788-53 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-788-53) |
NDC Code | 43353-788-53 |
Proprietary Name | quetiapine fumarate |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-788-53) |
Product NDC | 43353-788 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | quetiapine fumarate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120327 |
Marketing Category Name | ANDA |
Labeler Name | Aphena Pharma Solutions - Tennessee, Inc. |
Substance Name | QUETIAPINE FUMARATE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Atypical Antipsychotic [EPC] |