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Escitalopram Oxalate
Escitalopram Oxalate - 51079-543-56 - (escitalopram)
Drug Information of Escitalopram Oxalate
| Product NDC: | 51079-543 |
| Proprietary Name: | Escitalopram Oxalate |
| Non Proprietary Name: | escitalopram |
| Active Ingredient(s): | 10 mg/1 & nbsp; escitalopram |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Escitalopram Oxalate
| Product NDC: | 51079-543 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021323 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020814 |
Package Information of Escitalopram Oxalate
| Package NDC: | 51079-543-56 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-543-56) > 30 TABLET, FILM COATED in 1 BLISTER PACK (51079-543-30) |
NDC Information of Escitalopram Oxalate
| NDC Code | 51079-543-56 |
| Proprietary Name | Escitalopram Oxalate |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-543-56) > 30 TABLET, FILM COATED in 1 BLISTER PACK (51079-543-30) |
| Product NDC | 51079-543 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | escitalopram |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020814 |
| Marketing Category Name | NDA |
| Labeler Name | Mylan Institutional Inc. |
| Substance Name | ESCITALOPRAM OXALATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
