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sotalol hydrochloride
sotalol hydrochloride - 0185-0170-01 - (sotalol hydrochloride)
Drug Information of sotalol hydrochloride
| Product NDC: | 0185-0170 |
| Proprietary Name: | sotalol hydrochloride |
| Non Proprietary Name: | sotalol hydrochloride |
| Active Ingredient(s): | 120 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: | 0185-0170 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075366 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000501 |
Package Information of sotalol hydrochloride
| Package NDC: | 0185-0170-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0185-0170-01) |
NDC Information of sotalol hydrochloride
| NDC Code | 0185-0170-01 |
| Proprietary Name | sotalol hydrochloride |
| Package Description | 100 TABLET in 1 BOTTLE (0185-0170-01) |
| Product NDC | 0185-0170 |
| 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 | Eon Labs, Inc. |
| Substance Name | SOTALOL HYDROCHLORIDE |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
