Product NDC: | 0603-2217 |
Proprietary Name: | Amitriptyline Hydrochloride |
Non Proprietary Name: | Amitriptyline Hydrochloride |
Active Ingredient(s): | 150 mg/1 & nbsp; Amitriptyline Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-2217 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040218 |
Marketing Category: | ANDA |
Start Marketing Date: | 19970911 |
Package NDC: | 0603-2217-21 |
Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-2217-21) |
NDC Code | 0603-2217-21 |
Proprietary Name | Amitriptyline Hydrochloride |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-2217-21) |
Product NDC | 0603-2217 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amitriptyline Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19970911 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
Strength Number | 150 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |