Home
>
National Drug Code (NDC)
>
sotalol hydrochloride
sotalol hydrochloride - 54868-4435-1 - (sotalol hydrochloride)
Drug Information of sotalol hydrochloride
| Product NDC: | 54868-4435 |
| 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: | 54868-4435 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075366 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20001204 |
Package Information of sotalol hydrochloride
| Package NDC: | 54868-4435-1 |
| Package Description: | 60 TABLET in 1 BOTTLE (54868-4435-1) |
NDC Information of sotalol hydrochloride
| NDC Code | 54868-4435-1 |
| Proprietary Name | sotalol hydrochloride |
| Package Description | 60 TABLET in 1 BOTTLE (54868-4435-1) |
| Product NDC | 54868-4435 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sotalol hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20001204 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | SOTALOL HYDROCHLORIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
