Product NDC: | 49884-056 |
Proprietary Name: | Imipramine Hydrochloride |
Non Proprietary Name: | Imipramine Hydrochloride |
Active Ingredient(s): | 50 mg/1 & nbsp; Imipramine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49884-056 |
Labeler Name: | Par Pharmaceutical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA088276 |
Marketing Category: | ANDA |
Start Marketing Date: | 19831021 |
Package NDC: | 49884-056-01 |
Package Description: | 100 TABLET in 1 BOTTLE (49884-056-01) |
NDC Code | 49884-056-01 |
Proprietary Name | Imipramine Hydrochloride |
Package Description | 100 TABLET in 1 BOTTLE (49884-056-01) |
Product NDC | 49884-056 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Imipramine Hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19831021 |
Marketing Category Name | ANDA |
Labeler Name | Par Pharmaceutical Inc. |
Substance Name | IMIPRAMINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |