| Product NDC: | 51672-5276 |
| Proprietary Name: | OVIDE |
| 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: | 51672-5276 |
| Labeler Name: | TARO PHARMACEUTICALS USA, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018613 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19820802 |
| Package NDC: | 51672-5276-4 |
| Package Description: | 1 BOTTLE in 1 CARTON (51672-5276-4) > 59 mL in 1 BOTTLE |
| NDC Code | 51672-5276-4 |
| Proprietary Name | OVIDE |
| Package Description | 1 BOTTLE in 1 CARTON (51672-5276-4) > 59 mL in 1 BOTTLE |
| Product NDC | 51672-5276 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MALATHION |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19820802 |
| Marketing Category Name | NDA |
| Labeler Name | TARO PHARMACEUTICALS USA, INC. |
| Substance Name | MALATHION |
| Strength Number | .005 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |