Product NDC: | 16590-963 |
Proprietary Name: | IMIPRAMINE PAMOATE |
Non Proprietary Name: | IMIPRAMINE PAMOATE |
Active Ingredient(s): | 75 mg/1 & nbsp; IMIPRAMINE PAMOATE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-963 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017090 |
Marketing Category: | NDA |
Start Marketing Date: | 20091015 |
Package NDC: | 16590-963-60 |
Package Description: | 60 CAPSULE in 1 BOTTLE (16590-963-60) |
NDC Code | 16590-963-60 |
Proprietary Name | IMIPRAMINE PAMOATE |
Package Description | 60 CAPSULE in 1 BOTTLE (16590-963-60) |
Product NDC | 16590-963 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | IMIPRAMINE PAMOATE |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20091015 |
Marketing Category Name | NDA |
Labeler Name | STAT RX USA LLC |
Substance Name | IMIPRAMINE PAMOATE |
Strength Number | 75 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |