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Riluzole
Riluzole - 62756-538-18 - (Riluzole)
Drug Information of Riluzole
| Product NDC: | 62756-538 |
| Proprietary Name: | Riluzole |
| Non Proprietary Name: | Riluzole |
| Active Ingredient(s): | 50 mg/1 & nbsp; Riluzole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Riluzole
| Product NDC: | 62756-538 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091417 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130618 |
Package Information of Riluzole
| Package NDC: | 62756-538-18 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (62756-538-18) |
NDC Information of Riluzole
| NDC Code | 62756-538-18 |
| Proprietary Name | Riluzole |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (62756-538-18) |
| Product NDC | 62756-538 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Riluzole |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130618 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | RILUZOLE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzothiazole [EPC],Benzothiazoles [Chemical/Ingredient] |
