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risperidone
risperidone - 49349-619-29 - (risperidone)
Drug Information of risperidone
| Product NDC: | 49349-619 |
| Proprietary Name: | risperidone |
| Non Proprietary Name: | risperidone |
| Active Ingredient(s): | 2 mg/1 & nbsp; risperidone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of risperidone
| Product NDC: | 49349-619 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078040 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130501 |
Package Information of risperidone
| Package NDC: | 49349-619-29 |
| Package Description: | 360 TABLET, FILM COATED in 1 CANISTER (49349-619-29) |
NDC Information of risperidone
| NDC Code | 49349-619-29 |
| Proprietary Name | risperidone |
| Package Description | 360 TABLET, FILM COATED in 1 CANISTER (49349-619-29) |
| Product NDC | 49349-619 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | risperidone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | RISPERIDONE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC] |
