Ivermectin Tablet
Merck Sharp & Dohme LLC
Open FDA's page for this record- Discontinued date
- 09/29/2026
- Update type
- New
- Initial posting date
- 09/29/2026
- Package NDC
- 0006-0032-01
- Generic name
- Ivermectin Tablet
- Contact info
- 800-672-6372
- Related info
- Product will be discontinued on 10/31/2026
- Update date
- 09/29/2026
- Dosage form
- Tablet
- Presentation
- STROMECTOL, Tablet, 3 mg (NDC 0006-0032-01)
- Company name
- Merck Sharp & Dohme LLC
- Status
- To Be Discontinued
- Therapeutic category
- Anti-Infective
- Harmonized identifiers (openFDA)
- Application number
- NDA050742
- Brand name
- STROMECTOL
- Generic name
- IVERMECTIN
- Manufacturer name
- Merck Sharp & Dohme LLC
- Product NDC
- 0006-0032
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- ORAL
- Substance name
- IVERMECTIN
- RxCUI
- 261314, 311207
- SPL ID
- 200e22cc-3187-4a71-b8e1-73d90edab8bf
- SPL set ID
- 681888c9-af79-4b7d-ae80-c3f4f6f1effd
- Package NDC
- 0006-0032-20, 0006-0032-01
- Nui
- N0000175484, N0000181811
- Pharm class epc
- Antiparasitic [EPC], Pediculicide [EPC]
- UNII
- 8883YP2R6D