Product NDC: | 51079-133 |
Proprietary Name: | Amitriptyline Hydrochloride |
Non Proprietary Name: | amitriptyline hydrochloride |
Active Ingredient(s): | 50 mg/1 & nbsp; amitriptyline hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51079-133 |
Labeler Name: | Mylan Institutional Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA086009 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130313 |
Package NDC: | 51079-133-63 |
Package Description: | 30 TABLET, FILM COATED in 1 DOSE PACK (51079-133-63) |
NDC Code | 51079-133-63 |
Proprietary Name | Amitriptyline Hydrochloride |
Package Description | 30 TABLET, FILM COATED in 1 DOSE PACK (51079-133-63) |
Product NDC | 51079-133 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | amitriptyline hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20130313 |
Marketing Category Name | ANDA |
Labeler Name | Mylan Institutional Inc. |
Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |