Product NDC: | 24236-006 |
Proprietary Name: | AMITRIPTYLINE HYDROCHLORIDE |
Non Proprietary Name: | AMITRIPTYLINE HYDROCHLORIDE |
Active Ingredient(s): | 25 mg/1 & nbsp; AMITRIPTYLINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24236-006 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040218 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101213 |
Package NDC: | 24236-006-02 |
Package Description: | 30 TABLET in 1 BLISTER PACK (24236-006-02) |
NDC Code | 24236-006-02 |
Proprietary Name | AMITRIPTYLINE HYDROCHLORIDE |
Package Description | 30 TABLET in 1 BLISTER PACK (24236-006-02) |
Product NDC | 24236-006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | AMITRIPTYLINE HYDROCHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20101213 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |