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Trazodone Hydrochloride
Trazodone Hydrochloride - 21695-133-60 - (Trazodone)
Drug Information of Trazodone Hydrochloride
| Product NDC: | 21695-133 |
| Proprietary Name: | Trazodone Hydrochloride |
| Non Proprietary Name: | Trazodone |
| Active Ingredient(s): | 50 mg/1 & nbsp; Trazodone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trazodone Hydrochloride
| Product NDC: | 21695-133 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071523 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19871211 |
Package Information of Trazodone Hydrochloride
| Package NDC: | 21695-133-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (21695-133-60) |
NDC Information of Trazodone Hydrochloride
| NDC Code | 21695-133-60 |
| Proprietary Name | Trazodone Hydrochloride |
| Package Description | 60 TABLET in 1 BOTTLE (21695-133-60) |
| Product NDC | 21695-133 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trazodone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19871211 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | TRAZODONE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC] |
