Home
>
National Drug Code (NDC)
>
Sorine
Sorine - 0245-0015-11 - (Sotalol Hydrochloride)
Drug Information of Sorine
| Product NDC: | 0245-0015 |
| Proprietary Name: | Sorine |
| Non Proprietary Name: | Sotalol Hydrochloride |
| Active Ingredient(s): | 240 mg/1 & nbsp; Sotalol Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sorine
| Product NDC: | 0245-0015 |
| Labeler Name: | Upsher-Smith Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075500 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110215 |
Package Information of Sorine
| Package NDC: | 0245-0015-11 |
| Package Description: | 100 TABLET in 1 BOTTLE (0245-0015-11) |
NDC Information of Sorine
| NDC Code | 0245-0015-11 |
| Proprietary Name | Sorine |
| Package Description | 100 TABLET in 1 BOTTLE (0245-0015-11) |
| Product NDC | 0245-0015 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sotalol Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110215 |
| Marketing Category Name | ANDA |
| Labeler Name | Upsher-Smith Laboratories, Inc. |
| Substance Name | SOTALOL HYDROCHLORIDE |
| Strength Number | 240 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
