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Quetiapine fumarate
Quetiapine fumarate - 47335-902-83 - (Quetiapine fumarate)
Drug Information of Quetiapine fumarate
| Product NDC: | 47335-902 |
| 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) |
Labeler Information of Quetiapine fumarate
| Product NDC: | 47335-902 |
| Labeler Name: | Sun Pharma Global FZE |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201190 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120328 |
Package Information of Quetiapine fumarate
| Package NDC: | 47335-902-83 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (47335-902-83) |
NDC Information of Quetiapine fumarate
| NDC Code | 47335-902-83 |
| Proprietary Name | Quetiapine fumarate |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (47335-902-83) |
| Product NDC | 47335-902 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Quetiapine fumarate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120328 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global FZE |
| Substance Name | QUETIAPINE FUMARATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
