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FDA Approval

Permethrin

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Effective Date
October 1, 2021
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Permethrin(50 mg in 1 g)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Permethrin

Product Details

NDC Product Code
45802-269
Application Number
ANDA076369
Marketing Category
ANDA (C73584)
Route of Administration
TOPICAL
Effective Date
January 10, 2017
BUTYLATED HYDROXYTOLUENEInactive
Code: 1P9D0Z171KClass: IACT
LANOLIN ALCOHOLSInactive
Code: 884C3FA9HEClass: IACT
CETETH-20Inactive
Code: I835H2IHHXClass: IACT
MEDIUM-CHAIN TRIGLYCERIDESInactive
Code: C9H2L21V7UClass: IACT
GLYCERYL MONOSTEARATEInactive
Code: 230OU9XXE4Class: IACT
ISOPROPYL MYRISTATEInactive
Code: 0RE8K4LNJSClass: IACT
Code: 509F88P9SZClass: ACTIBQuantity: 50 mg in 1 g
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)Inactive
Code: HHT01ZNK31Class: IACT
GLYCERINInactive
Code: PDC6A3C0OXClass: IACT
MINERAL OILInactive
Code: T5L8T28FGPClass: IACT
WATERInactive
Code: 059QF0KO0RClass: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32IClass: IACT
FORMALDEHYDEInactive
Code: 1HG84L3525Class: IACT
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