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Modafinil
Modafinil - 65862-601-90 - (Modafinil)
Drug Information of Modafinil
| Product NDC: | 65862-601 |
| Proprietary Name: | Modafinil |
| Non Proprietary Name: | Modafinil |
| Active Ingredient(s): | 100 mg/1 & nbsp; Modafinil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Modafinil
| Product NDC: | 65862-601 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202566 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120927 |
Package Information of Modafinil
| Package NDC: | 65862-601-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (65862-601-90) |
NDC Information of Modafinil
| NDC Code | 65862-601-90 |
| Proprietary Name | Modafinil |
| Package Description | 90 TABLET in 1 BOTTLE (65862-601-90) |
| Product NDC | 65862-601 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Modafinil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120927 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | MODAFINIL |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC] |
