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EMEND
EMEND - 0006-0461-12 - (aprepitant)
Drug Information of EMEND
| Product NDC: | 0006-0461 |
| Proprietary Name: | EMEND |
| Non Proprietary Name: | aprepitant |
| Active Ingredient(s): | 80 mg/1 & nbsp; aprepitant |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EMEND
| Product NDC: | 0006-0461 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021549 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030326 |
Package Information of EMEND
| Package NDC: | 0006-0461-12 |
| Package Description: | 2 CAPSULE in 1 DOSE PACK (0006-0461-12) |
NDC Information of EMEND
| NDC Code | 0006-0461-12 |
| Proprietary Name | EMEND |
| Package Description | 2 CAPSULE in 1 DOSE PACK (0006-0461-12) |
| Product NDC | 0006-0461 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | aprepitant |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20030326 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | APREPITANT |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Neurokinin 1 Antagonists [MoA],Substance P/Neurokinin-1 Receptor Antagonist [EPC] |
