Product NDC: | 10544-110 |
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: | 10544-110 |
Labeler Name: | Blenheim Pharmacal, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA085968 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100303 |
Package NDC: | 10544-110-30 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (10544-110-30) |
NDC Code | 10544-110-30 |
Proprietary Name | Amitriptyline Hydrochloride |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (10544-110-30) |
Product NDC | 10544-110 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amitriptyline Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100303 |
Marketing Category Name | ANDA |
Labeler Name | Blenheim Pharmacal, Inc. |
Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |