Trazodone Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp.. The primary component is Trazodone Hydrochloride.
| Product ID | 21695-133_370453cb-7636-43f2-93f0-e8714884fab4 |
| NDC | 21695-133 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Trazodone Hydrochloride |
| Generic Name | Trazodone |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1987-12-11 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA071523 |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | TRAZODONE HYDROCHLORIDE |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | Serotonin Reuptake Inhibitor [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 1987-12-11 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA071523 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-12-11 |
| Inactivation Date | 2019-09-24 |
| Marketing Category | ANDA |
| Application Number | ANDA071523 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-12-11 |
| Inactivation Date | 2019-09-24 |
| Marketing Category | ANDA |
| Application Number | ANDA071523 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-12-11 |
| Inactivation Date | 2019-09-24 |
| Marketing Category | ANDA |
| Application Number | ANDA071523 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-12-11 |
| Inactivation Date | 2019-09-24 |
| Ingredient | Strength |
|---|---|
| TRAZODONE HYDROCHLORIDE | 50 mg/1 |
| SPL SET ID: | 6f43cdc2-4f8e-4a5f-976a-d3aaac65593d |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |