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Lexapro
Lexapro - 54868-4775-0 - (escitalopram oxalate)
Drug Information of Lexapro
| Product NDC: | 54868-4775 |
| Proprietary Name: | Lexapro |
| Non Proprietary Name: | escitalopram oxalate |
| Active Ingredient(s): | 20 mg/1 & nbsp; escitalopram oxalate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lexapro
| Product NDC: | 54868-4775 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021323 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090415 |
Package Information of Lexapro
| Package NDC: | 54868-4775-0 |
| Package Description: | 10 TABLET in 1 BOTTLE, PLASTIC (54868-4775-0) |
NDC Information of Lexapro
| NDC Code | 54868-4775-0 |
| Proprietary Name | Lexapro |
| Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (54868-4775-0) |
| Product NDC | 54868-4775 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | escitalopram oxalate |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090415 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ESCITALOPRAM OXALATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
