Ivermectin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Edenbridge Pharmaceuticals Llc.. The primary component is Ivermectin.
Product ID | 42799-806_5ee11d40-87d8-4c2d-a39a-d42e963b5b3f |
NDC | 42799-806 |
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 | Edenbridge Pharmaceuticals LLC. |
Substance Name | IVERMECTIN |
Active Ingredient Strength | 3 mg/1 |
Pharm Classes | Antiparasitic [EPC],Pediculicide [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2014-11-15 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA204154 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-11-15 |
Ingredient | Strength |
---|---|
IVERMECTIN | 3 mg/1 |
SPL SET ID: | 847a1dd7-d65b-4a0e-a67d-d90392059dac |
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 |