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Seroquel
Seroquel - 49349-241-02 - (Seroquel)
Drug Information of Seroquel
| Product NDC: | 49349-241 |
| Proprietary Name: | Seroquel |
| Non Proprietary Name: | Seroquel |
| Active Ingredient(s): | 150 mg/1 & nbsp; Seroquel |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Seroquel
| Product NDC: | 49349-241 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022047 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110323 |
Package Information of Seroquel
| Package NDC: | 49349-241-02 |
| Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-241-02) |
NDC Information of Seroquel
| NDC Code | 49349-241-02 |
| Proprietary Name | Seroquel |
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-241-02) |
| Product NDC | 49349-241 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Seroquel |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20110323 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | QUETIAPINE FUMARATE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
