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Escitalopram
Escitalopram - 68645-447-70 - (Escitalopram)
Drug Information of Escitalopram
| Product NDC: | 68645-447 |
| Proprietary Name: | Escitalopram |
| Non Proprietary Name: | Escitalopram |
| Active Ingredient(s): | 20 mg/1 & nbsp; Escitalopram |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Escitalopram
| Product NDC: | 68645-447 |
| Labeler Name: | Legacy Pharmaceutical Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078604 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120911 |
Package Information of Escitalopram
| Package NDC: | 68645-447-70 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (68645-447-70) |
NDC Information of Escitalopram
| NDC Code | 68645-447-70 |
| Proprietary Name | Escitalopram |
| Package Description | 30 TABLET in 1 BLISTER PACK (68645-447-70) |
| Product NDC | 68645-447 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Escitalopram |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120911 |
| Marketing Category Name | ANDA |
| Labeler Name | Legacy Pharmaceutical Packaging |
| Substance Name | ESCITALOPRAM OXALATE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
