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Celexa
Celexa - 54868-4159-4 - (citalopram hydrobromide)
Drug Information of Celexa
| Product NDC: | 54868-4159 |
| Proprietary Name: | Celexa |
| Non Proprietary Name: | citalopram hydrobromide |
| Active Ingredient(s): | 20 mg/1 & nbsp; citalopram hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Celexa
| Product NDC: | 54868-4159 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020822 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20001128 |
Package Information of Celexa
| Package NDC: | 54868-4159-4 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (54868-4159-4) |
NDC Information of Celexa
| NDC Code | 54868-4159-4 |
| Proprietary Name | Celexa |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (54868-4159-4) |
| Product NDC | 54868-4159 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | citalopram hydrobromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20001128 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | CITALOPRAM HYDROBROMIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
