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Risperidone Oral Disintegrate Tablets
Risperidone Oral Disintegrate Tablets - 63304-643-69 - (Risperidone Oral Disintegrate Tablets)
Drug Information of Risperidone Oral Disintegrate Tablets
| Product NDC: | 63304-643 |
| Proprietary Name: | Risperidone Oral Disintegrate Tablets |
| Non Proprietary Name: | Risperidone Oral Disintegrate Tablets |
| Active Ingredient(s): | 3 mg/1 & nbsp; Risperidone Oral Disintegrate Tablets |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Risperidone Oral Disintegrate Tablets
| Product NDC: | 63304-643 |
| Labeler Name: | Ranbaxy Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078474 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100818 |
Package Information of Risperidone Oral Disintegrate Tablets
| Package NDC: | 63304-643-69 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (63304-643-69) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63304-643-11) |
NDC Information of Risperidone Oral Disintegrate Tablets
| NDC Code | 63304-643-69 |
| Proprietary Name | Risperidone Oral Disintegrate Tablets |
| Package Description | 1 BLISTER PACK in 1 CARTON (63304-643-69) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (63304-643-11) |
| Product NDC | 63304-643 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Risperidone Oral Disintegrate Tablets |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20100818 |
| Marketing Category Name | ANDA |
| Labeler Name | Ranbaxy Pharmaceuticals Inc. |
| Substance Name | RISPERIDONE |
| Strength Number | 3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
