Product NDC: | 54569-1470 |
Proprietary Name: | Trazodone Hydrochloride |
Non Proprietary Name: | Trazodone Hydrochloride |
Active Ingredient(s): | 50 mg/1 & nbsp; Trazodone Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-1470 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA072192 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100530 |
Package NDC: | 54569-1470-0 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54569-1470-0) |
NDC Code | 54569-1470-0 |
Proprietary Name | Trazodone Hydrochloride |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54569-1470-0) |
Product NDC | 54569-1470 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Trazodone Hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100530 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | TRAZODONE HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC] |