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Citalopram
Citalopram - 49349-517-20 - (Citalopram)
Drug Information of Citalopram
| Product NDC: | 49349-517 |
| Proprietary Name: | Citalopram |
| Non Proprietary Name: | Citalopram |
| Active Ingredient(s): | 40 mg/1 & nbsp; Citalopram |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Citalopram
| Product NDC: | 49349-517 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077031 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130304 |
Package Information of Citalopram
| Package NDC: | 49349-517-20 |
| Package Description: | 100 TABLET in 1 VIAL (49349-517-20) |
NDC Information of Citalopram
| NDC Code | 49349-517-20 |
| Proprietary Name | Citalopram |
| Package Description | 100 TABLET in 1 VIAL (49349-517-20) |
| Product NDC | 49349-517 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Citalopram |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130304 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | CITALOPRAM HYDROBROMIDE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
