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Sotalol Hydrochloride
Sotalol Hydrochloride - 0603-5769-32 - (Sotalol Hydrochloride)
Drug Information of Sotalol Hydrochloride
| Product NDC: | 0603-5769 |
| Proprietary Name: | Sotalol Hydrochloride |
| Non Proprietary Name: | Sotalol Hydrochloride |
| Active Ingredient(s): | 80 mg/1 & nbsp; Sotalol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sotalol Hydrochloride
| Product NDC: | 0603-5769 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075563 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031107 |
Package Information of Sotalol Hydrochloride
| Package NDC: | 0603-5769-32 |
| Package Description: | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5769-32) |
NDC Information of Sotalol Hydrochloride
| NDC Code | 0603-5769-32 |
| Proprietary Name | Sotalol Hydrochloride |
| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (0603-5769-32) |
| Product NDC | 0603-5769 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sotalol Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20031107 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | SOTALOL HYDROCHLORIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
