MALATHION

Product NDC

51672-5277

11-digit product format

516725277

Labeler code

51672

Product ID

51672-5277_a3510c3b-9538-4ce6-9736-95f9079c71c8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MALATHION

Dosage form

LOTION

Route

TOPICAL

Labeler

TARO PHARMACEUTICALS U.S.A., INC.

Application

NDA018613

Marketing category

NDA

Marketing start

2009-08-02

Marketing end

0000-00-00

Substance

MALATHION

Active strength

0 g/mL

Pharmacologic classes

Cholinesterase Inhibitors [MoA],Cholinesterase Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record