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Thioridazine Hydrochloride
Thioridazine Hydrochloride - 0378-0614-10 - (thioridazine hydrochloride)
Drug Information of Thioridazine Hydrochloride
| Product NDC: | 0378-0614 |
| Proprietary Name: | Thioridazine Hydrochloride |
| Non Proprietary Name: | thioridazine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; thioridazine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Thioridazine Hydrochloride
| Product NDC: | 0378-0614 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088004 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19830315 |
Package Information of Thioridazine Hydrochloride
| Package NDC: | 0378-0614-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0614-10) |
NDC Information of Thioridazine Hydrochloride
| NDC Code | 0378-0614-10 |
| Proprietary Name | Thioridazine Hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0614-10) |
| Product NDC | 0378-0614 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | thioridazine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19830315 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | THIORIDAZINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
