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Trifluoperazine Hydrochloride
Trifluoperazine Hydrochloride - 0781-1032-01 - (Trifluoperazine Hydrochloride)
Drug Information of Trifluoperazine Hydrochloride
| Product NDC: | 0781-1032 |
| Proprietary Name: | Trifluoperazine Hydrochloride |
| Non Proprietary Name: | Trifluoperazine Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Trifluoperazine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Trifluoperazine Hydrochloride
| Product NDC: | 0781-1032 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085786 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19811120 |
Package Information of Trifluoperazine Hydrochloride
| Package NDC: | 0781-1032-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0781-1032-01) |
NDC Information of Trifluoperazine Hydrochloride
| NDC Code | 0781-1032-01 |
| Proprietary Name | Trifluoperazine Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0781-1032-01) |
| Product NDC | 0781-1032 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Trifluoperazine Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19811120 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | TRIFLUOPERAZINE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
