Home
>
National Drug Code (NDC)
>
Mexiletine Hydrochloride
Mexiletine Hydrochloride - 0093-8740-01 - (Mexiletine Hydrochloride)
Drug Information of Mexiletine Hydrochloride
| Product NDC: | 0093-8740 |
| Proprietary Name: | Mexiletine Hydrochloride |
| Non Proprietary Name: | Mexiletine Hydrochloride |
| Active Ingredient(s): | 200 mg/1 & nbsp; Mexiletine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mexiletine Hydrochloride
| Product NDC: | 0093-8740 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074377 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950605 |
Package Information of Mexiletine Hydrochloride
| Package NDC: | 0093-8740-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0093-8740-01) |
NDC Information of Mexiletine Hydrochloride
| NDC Code | 0093-8740-01 |
| Proprietary Name | Mexiletine Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (0093-8740-01) |
| Product NDC | 0093-8740 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mexiletine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19950605 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | MEXILETINE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
