Product NDC: | 51672-5277 |
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) |
Product NDC: | 51672-5277 |
Labeler Name: | TARO PHARMACEUTICALS U.S.A., INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018613 |
Marketing Category: | NDA |
Start Marketing Date: | 20090802 |
Package NDC: | 51672-5277-4 |
Package Description: | 1 BOTTLE in 1 CARTON (51672-5277-4) > 59 mL in 1 BOTTLE |
NDC Code | 51672-5277-4 |
Proprietary Name | MALATHION |
Package Description | 1 BOTTLE in 1 CARTON (51672-5277-4) > 59 mL in 1 BOTTLE |
Product NDC | 51672-5277 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | MALATHION |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20090802 |
Marketing Category Name | NDA |
Labeler Name | TARO PHARMACEUTICALS U.S.A., INC. |
Substance Name | MALATHION |
Strength Number | .005 |
Strength Unit | g/mL |
Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |