Product NDC: | 54868-4023 |
Proprietary Name: | CLOMIPRAMINE HYDROCHLORIDE |
Non Proprietary Name: | Clomipramine Hydrochloride |
Active Ingredient(s): | 50 mg/1 & nbsp; Clomipramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4023 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074694 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050928 |
Package NDC: | 54868-4023-0 |
Package Description: | 60 CAPSULE in 1 BOTTLE (54868-4023-0) |
NDC Code | 54868-4023-0 |
Proprietary Name | CLOMIPRAMINE HYDROCHLORIDE |
Package Description | 60 CAPSULE in 1 BOTTLE (54868-4023-0) |
Product NDC | 54868-4023 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clomipramine Hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20050928 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CLOMIPRAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |