Product NDC: | 35356-720 |
Proprietary Name: | Citalopram |
Non Proprietary Name: | Citalopram |
Active Ingredient(s): | 20 mg/1 & nbsp; Citalopram |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-720 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077534 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110101 |
Package NDC: | 35356-720-30 |
Package Description: | 30 TABLET in 1 BOTTLE (35356-720-30) |
NDC Code | 35356-720-30 |
Proprietary Name | Citalopram |
Package Description | 30 TABLET in 1 BOTTLE (35356-720-30) |
Product NDC | 35356-720 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Citalopram |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110101 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | CITALOPRAM HYDROBROMIDE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |