Mexiletine Hydrochloride - Mexiletine Hydrochloride
Navigation: NDC > Supplier starting with: T > TEVA PHARMACEUTICALS USA INC| Field | Value |
|---|---|
| NDC Code: | 0093-8739 |
| Proprietary Name: | Mexiletine Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Mexiletine Hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 05-06-1995 |
| Category Name: | ANDA |
| Application Number: | ANDA074377 |
| Labeler: | TEVA PHARMACEUTICALS USA INC |
| Substance Name: | MEXILETINE HYDROCHLORIDE |
| Active Numerator Strength: | 150 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Antiarrhythmic [EPC] |
| DEA Schedule: |