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Trazodone Hydrochloride
Trazodone Hydrochloride - 53489-517-07 - (Trazodone Hydrochloride)
Drug Information of Trazodone Hydrochloride
| Product NDC: | 53489-517 |
| Proprietary Name: | Trazodone Hydrochloride |
| Non Proprietary Name: | Trazodone Hydrochloride |
| Active Ingredient(s): | 150 mg/1 & nbsp; Trazodone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trazodone Hydrochloride
| Product NDC: | 53489-517 |
| Labeler Name: | Mutual Pharmaceutical Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073137 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930324 |
Package Information of Trazodone Hydrochloride
| Package NDC: | 53489-517-07 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-517-07) |
NDC Information of Trazodone Hydrochloride
| NDC Code | 53489-517-07 |
| Proprietary Name | Trazodone Hydrochloride |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-517-07) |
| Product NDC | 53489-517 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trazodone Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19930324 |
| Marketing Category Name | ANDA |
| Labeler Name | Mutual Pharmaceutical Company, Inc. |
| Substance Name | TRAZODONE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC] |
