| NDC Code | 53489-500-02 |
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| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-500-02) |
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| Product NDC | 53489-500 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Thioridazine Hydrochloride |
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| Non-Proprietary Name | Thioridazine Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 19881007 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA089953 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | THIORIDAZINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Phenothiazine [EPC], Phenothiazines [CS] |
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