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Perphenazine and Amitriptyline Hydrochloride
Perphenazine and Amitriptyline Hydrochloride - 49349-622-02 - (Perphenazine and Amitriptyline Hydrochloride)
Drug Information of Perphenazine and Amitriptyline Hydrochloride
| Product NDC: | 49349-622 |
| Proprietary Name: | Perphenazine and Amitriptyline Hydrochloride |
| Non Proprietary Name: | Perphenazine and Amitriptyline Hydrochloride |
| Active Ingredient(s): | 50; 4 mg/1; mg/1 & nbsp; Perphenazine and Amitriptyline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Perphenazine and Amitriptyline Hydrochloride
| Product NDC: | 49349-622 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071443 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111207 |
Package Information of Perphenazine and Amitriptyline Hydrochloride
| Package NDC: | 49349-622-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-622-02) |
NDC Information of Perphenazine and Amitriptyline Hydrochloride
| NDC Code | 49349-622-02 |
| Proprietary Name | Perphenazine and Amitriptyline Hydrochloride |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-622-02) |
| Product NDC | 49349-622 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Perphenazine and Amitriptyline Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111207 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | AMITRIPTYLINE HYDROCHLORIDE; PERPHENAZINE |
| Strength Number | 50; 4 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient],Tricyclic Antidepressant [EPC] |
