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STROMECTOL
STROMECTOL - 0006-0032-20 - (ivermectin)
Drug Information of STROMECTOL
| Product NDC: | 0006-0032 |
| Proprietary Name: | STROMECTOL |
| Non Proprietary Name: | ivermectin |
| Active Ingredient(s): | 3 mg/1 & nbsp; ivermectin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of STROMECTOL
| Product NDC: | 0006-0032 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050742 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961122 |
Package Information of STROMECTOL
| Package NDC: | 0006-0032-20 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0006-0032-20) > 10 TABLET in 1 BLISTER PACK |
NDC Information of STROMECTOL
| NDC Code | 0006-0032-20 |
| Proprietary Name | STROMECTOL |
| Package Description | 2 BLISTER PACK in 1 CARTON (0006-0032-20) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 0006-0032 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ivermectin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19961122 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | IVERMECTIN |
| Strength Number | 3 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiparasitic [EPC],Pediculicide [EPC] |
