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