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Clomipramine Hydrochloride
Clomipramine Hydrochloride - 0781-2027-31 - (Clomipramine Hydrochloride)
Drug Information of Clomipramine Hydrochloride
| Product NDC: | 0781-2027 |
| Proprietary Name: | Clomipramine Hydrochloride |
| Non Proprietary Name: | Clomipramine Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Clomipramine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clomipramine Hydrochloride
| Product NDC: | 0781-2027 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074364 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960329 |
Package Information of Clomipramine Hydrochloride
| Package NDC: | 0781-2027-31 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (0781-2027-31) |
NDC Information of Clomipramine Hydrochloride
| NDC Code | 0781-2027-31 |
| Proprietary Name | Clomipramine Hydrochloride |
| Package Description | 30 CAPSULE in 1 BOTTLE (0781-2027-31) |
| Product NDC | 0781-2027 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clomipramine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19960329 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CLOMIPRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
