Product NDC: | 65862-074 |
Proprietary Name: | Citalopram Hydrobromide |
Non Proprietary Name: | Citalopram Hydrobromide |
Active Ingredient(s): | 10 mg/5mL & nbsp; Citalopram Hydrobromide |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65862-074 |
Labeler Name: | Aurobindo Pharma Limited |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077812 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060828 |
Package NDC: | 65862-074-24 |
Package Description: | 240 mL in 1 BOTTLE (65862-074-24) |
NDC Code | 65862-074-24 |
Proprietary Name | Citalopram Hydrobromide |
Package Description | 240 mL in 1 BOTTLE (65862-074-24) |
Product NDC | 65862-074 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Citalopram Hydrobromide |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20060828 |
Marketing Category Name | ANDA |
Labeler Name | Aurobindo Pharma Limited |
Substance Name | CITALOPRAM HYDROBROMIDE |
Strength Number | 10 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |