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Nefazodone Hydrochloride
Nefazodone Hydrochloride - 21695-176-30 - (Nefazodone Hydrochloride)
Drug Information of Nefazodone Hydrochloride
| Product NDC: | 21695-176 |
| Proprietary Name: | Nefazodone Hydrochloride |
| Non Proprietary Name: | Nefazodone Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Nefazodone Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nefazodone Hydrochloride
| Product NDC: | 21695-176 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076037 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030916 |
Package Information of Nefazodone Hydrochloride
| Package NDC: | 21695-176-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-176-30) |
NDC Information of Nefazodone Hydrochloride
| NDC Code | 21695-176-30 |
| Proprietary Name | Nefazodone Hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (21695-176-30) |
| Product NDC | 21695-176 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nefazodone Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030916 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | NEFAZODONE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC] |
