NDC 51672-4211

Ivermectin

Ivermectin

Ivermectin is a Topical Lotion in the Human Prescription Drug category. It is labeled and distributed by Taro Pharmaceuticals U.s.a., Inc.. The primary component is Ivermectin.

Product ID51672-4211_92921d55-1976-4d38-8e19-5c1705f052b2
NDC51672-4211
Product TypeHuman Prescription Drug
Proprietary NameIvermectin
Generic NameIvermectin
Dosage FormLotion
Route of AdministrationTOPICAL
Marketing Start Date2020-05-06
Marketing CategoryANDA / ANDA
Application NumberANDA210720
Labeler NameTaro Pharmaceuticals U.S.A., Inc.
Substance NameIVERMECTIN
Active Ingredient Strength5 mg/g
Pharm ClassesAntiparasitic [EPC],Pediculicide [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 51672-4211-8

1 TUBE in 1 CARTON (51672-4211-8) > 117 g in 1 TUBE
Marketing Start Date2020-05-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51672-4211-8 [51672421108]

Ivermectin LOTION
Marketing CategoryANDA
Application NumberANDA210720
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-05-06

Drug Details

NDC Crossover Matching brand name "Ivermectin" or generic name "Ivermectin"

NDCBrand NameGeneric Name
0363-4230IvermectinIvermectin
0574-2107IvermectinIVERMECTIN
0591-4052IvermectinIvermectin
11822-4230IvermectinIvermectin
42799-806IvermectinIvermectin
50090-5587IvermectinIvermectin
51316-423IvermectinIvermectin
51672-4211IvermectinIvermectin
51672-4230IvermectinIvermectin
63629-7275IvermectinIvermectin
63629-8754IvermectinIvermectin
66993-948IvermectinIVERMECTIN
68071-2242IvermectinIvermectin
76413-155IvermectinIvermectin
79903-154IvermectinIvermectin
24338-183SkliceIVERMECTIN
24338-185Skliceivermectin
0299-3823SOOLANTRAIVERMECTIN
0006-0032STROMECTOLivermectin
55695-019STROMECTOLivermectin

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.