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Disopyramide Phosphate
Disopyramide Phosphate - 0093-3129-01 - (Disopyramide Phosphate)
Drug Information of Disopyramide Phosphate
| Product NDC: | 0093-3129 |
| Proprietary Name: | Disopyramide Phosphate |
| Non Proprietary Name: | Disopyramide Phosphate |
| Active Ingredient(s): | 150 mg/1 & nbsp; Disopyramide Phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Disopyramide Phosphate
| Product NDC: | 0093-3129 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070102 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19900930 |
Package Information of Disopyramide Phosphate
| Package NDC: | 0093-3129-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0093-3129-01) |
NDC Information of Disopyramide Phosphate
| NDC Code | 0093-3129-01 |
| Proprietary Name | Disopyramide Phosphate |
| Package Description | 100 CAPSULE in 1 BOTTLE (0093-3129-01) |
| Product NDC | 0093-3129 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Disopyramide Phosphate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19900930 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | DISOPYRAMIDE PHOSPHATE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
