Malathion - 68022-0001-1 - (Malathion)

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Drug Information of Malathion

Product NDC: 68022-0001
Proprietary Name: Malathion
Non Proprietary Name: Malathion
Active Ingredient(s): .005    g/mL & nbsp;   Malathion
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Malathion

Product NDC: 68022-0001
Labeler Name: Suven Life Sciences Ltd
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091559
Marketing Category: ANDA
Start Marketing Date: 20110523

Package Information of Malathion

Package NDC: 68022-0001-1
Package Description: 1 BOTTLE in 1 CARTON (68022-0001-1) > 59 mL in 1 BOTTLE

NDC Information of Malathion

NDC Code 68022-0001-1
Proprietary Name Malathion
Package Description 1 BOTTLE in 1 CARTON (68022-0001-1) > 59 mL in 1 BOTTLE
Product NDC 68022-0001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Malathion
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110523
Marketing Category Name ANDA
Labeler Name Suven Life Sciences Ltd
Substance Name MALATHION
Strength Number .005
Strength Unit g/mL
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Malathion


General Information