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Natroba
Natroba - 52246-929-04 - (spinosad)
Drug Information of Natroba
| Product NDC: | 52246-929 |
| Proprietary Name: | Natroba |
| Non Proprietary Name: | spinosad |
| Active Ingredient(s): | 9 mg/mL & nbsp; spinosad |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Natroba
| Product NDC: | 52246-929 |
| Labeler Name: | ParaPRO LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022408 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110125 |
Package Information of Natroba
| Package NDC: | 52246-929-04 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52246-929-04) > 120 mL in 1 BOTTLE, PLASTIC |
NDC Information of Natroba
| NDC Code | 52246-929-04 |
| Proprietary Name | Natroba |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52246-929-04) > 120 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 52246-929 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | spinosad |
| Dosage Form Name | SUSPENSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110125 |
| Marketing Category Name | NDA |
| Labeler Name | ParaPRO LLC |
| Substance Name | SPINOSAD |
| Strength Number | 9 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Pediculicide [EPC] |
