Home
>
National Drug Code (NDC)
>
sotalol hydrochloride
sotalol hydrochloride - 21695-397-30 - (sotalol hydrochloride)
Drug Information of sotalol hydrochloride
| Product NDC: | 21695-397 |
| 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: | 21695-397 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075366 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000501 |
Package Information of sotalol hydrochloride
| Package NDC: | 21695-397-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-397-30) |
NDC Information of sotalol hydrochloride
| NDC Code | 21695-397-30 |
| Proprietary Name | sotalol hydrochloride |
| Package Description | 30 TABLET in 1 BOTTLE (21695-397-30) |
| Product NDC | 21695-397 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sotalol hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20000501 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | SOTALOL HYDROCHLORIDE |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
