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quetiapine fumarate
quetiapine fumarate - 60505-3135-5 - (quetiapine fumarate)
Drug Information of quetiapine fumarate
| Product NDC: | 60505-3135 |
| Proprietary Name: | quetiapine fumarate |
| Non Proprietary Name: | quetiapine fumarate |
| Active Ingredient(s): | 200 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: | 60505-3135 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090960 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120327 |
Package Information of quetiapine fumarate
| Package NDC: | 60505-3135-5 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (60505-3135-5) |
NDC Information of quetiapine fumarate
| NDC Code | 60505-3135-5 |
| Proprietary Name | quetiapine fumarate |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (60505-3135-5) |
| Product NDC | 60505-3135 |
| 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 | Apotex Corp. |
| Substance Name | QUETIAPINE FUMARATE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
