Product NDC: | 0378-3075 |
Proprietary Name: | Clomipramine Hydrochloride |
Non Proprietary Name: | clomipramine hydrochloride |
Active Ingredient(s): | 75 mg/1 & nbsp; clomipramine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0378-3075 |
Labeler Name: | Mylan Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074947 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130118 |
Package NDC: | 0378-3075-01 |
Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3075-01) |
NDC Code | 0378-3075-01 |
Proprietary Name | Clomipramine Hydrochloride |
Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3075-01) |
Product NDC | 0378-3075 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clomipramine hydrochloride |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20130118 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Pharmaceuticals Inc. |
Substance Name | CLOMIPRAMINE HYDROCHLORIDE |
Strength Number | 75 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |