Home
>
National Drug Code (NDC)
>
Citalopram Hydrobromide
Citalopram Hydrobromide - 0054-0062-58 - (Citalopram Hydrobromide)
Drug Information of Citalopram Hydrobromide
| Product NDC: | 0054-0062 |
| 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) |
Labeler Information of Citalopram Hydrobromide
| Product NDC: | 0054-0062 |
| Labeler Name: | Roxane Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065178 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040525 |
Package Information of Citalopram Hydrobromide
| Package NDC: | 0054-0062-58 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0054-0062-58) > 240 mL in 1 BOTTLE, PLASTIC |
NDC Information of Citalopram Hydrobromide
| NDC Code | 0054-0062-58 |
| Proprietary Name | Citalopram Hydrobromide |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0054-0062-58) > 240 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 0054-0062 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Citalopram Hydrobromide |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20040525 |
| Marketing Category Name | ANDA |
| Labeler Name | Roxane Laboratories, Inc |
| Substance Name | CITALOPRAM HYDROBROMIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
