Ivermectin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Central Texas Community Health Centers. The primary component is Ivermectin.
| Product ID | 76413-155_ad836382-a68f-4794-b81b-c4e8f8748cf1 |
| NDC | 76413-155 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Ivermectin |
| Generic Name | Ivermectin |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-11-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA204154 |
| Labeler Name | Central Texas Community Health Centers |
| Substance Name | IVERMECTIN |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Antiparasitic [EPC],Pediculicide [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2018-03-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2014-11-15 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-12 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-12 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-12 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-12 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-12 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA204154 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2018-03-12 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| IVERMECTIN | 3 mg/1 |
| SPL SET ID: | 23bb1ccf-1a35-438d-a0df-3ecc4fa30033 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0363-4230 | Ivermectin | Ivermectin |
| 0574-2107 | Ivermectin | IVERMECTIN |
| 0591-4052 | Ivermectin | Ivermectin |
| 11822-4230 | Ivermectin | Ivermectin |
| 42799-806 | Ivermectin | Ivermectin |
| 50090-5587 | Ivermectin | Ivermectin |
| 51316-423 | Ivermectin | Ivermectin |
| 51672-4211 | Ivermectin | Ivermectin |
| 51672-4230 | Ivermectin | Ivermectin |
| 63629-7275 | Ivermectin | Ivermectin |
| 63629-8754 | Ivermectin | Ivermectin |
| 66993-948 | Ivermectin | IVERMECTIN |
| 68071-2242 | Ivermectin | Ivermectin |
| 76413-155 | Ivermectin | Ivermectin |
| 79903-154 | Ivermectin | Ivermectin |
| 24338-183 | Sklice | IVERMECTIN |
| 24338-185 | Sklice | ivermectin |
| 0299-3823 | SOOLANTRA | IVERMECTIN |
| 0006-0032 | STROMECTOL | ivermectin |
| 55695-019 | STROMECTOL | ivermectin |