Search by Drug Name or NDC
NDC 57664-0053-74 Trazodone Hydrochloride 150 mg/1 Details
Trazodone Hydrochloride 150 mg/1
Trazodone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is TRAZODONE HYDROCHLORIDE.
Product Information
| NDC | 57664-0053 |
|---|---|
| Product ID | 57664-053_f291a9f6-4b36-753c-e053-2a95a90a181a |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Trazodone Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Trazodone Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 150 |
| Active Ingredient Units | mg/1 |
| Substance Name | TRAZODONE HYDROCHLORIDE |
| Labeler Name | Sun Pharmaceutical Industries, Inc. |
| Pharmaceutical Class | Serotonin Reuptake Inhibitor [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA073137 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 57664-0053-74 (57664005374)
| NDC Package Code | 57664-053-74 |
|---|---|
| Billing NDC | 57664005374 |
| Package | 500 TABLET in 1 BOTTLE, PLASTIC (57664-053-74) |
| Marketing Start Date | 2022-10-03 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |