Nefazodone Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Nefazodone Hydrochloride.
| Product ID | 63629-7046_0bd4c34a-4f43-4c84-8b98-1d074cba97d5 |
| NDC | 63629-7046 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nefazodone Hydrochloride |
| Generic Name | Nefazodone Hydrochloride |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-09-16 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076037 |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | NEFAZODONE HYDROCHLORIDE |
| Active Ingredient Strength | 150 mg/1 |
| Pharm Classes | Serotonin Reuptake Inhibitor [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2022-02-08 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076037 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-18 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-25 |
| Marketing Category | ANDA |
| Application Number | ANDA076037 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-18 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-25 |
| Marketing Category | ANDA |
| Application Number | ANDA076037 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-18 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-25 |
| Marketing Category | ANDA |
| Application Number | ANDA076037 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-10-18 |
| Inactivation Date | 2020-01-31 |
| Reactivation Date | 2020-02-25 |
| Ingredient | Strength |
|---|---|
| NEFAZODONE HYDROCHLORIDE | 150 mg/1 |
| SPL SET ID: | 0bd4c34a-4f43-4c84-8b98-1d074cba97d5 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0093-1024 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 0093-1025 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 0093-1026 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 0093-7113 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 0093-7178 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 21695-174 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 21695-175 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 21695-176 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 21695-177 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 63629-7046 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 63629-7214 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 63629-7310 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 68788-7217 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 68788-7242 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |
| 68788-7246 | Nefazodone Hydrochloride | Nefazodone Hydrochloride |