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Pronto Plus
Pronto Plus - 63736-240-24 - (Pyrantel pamoate)
Drug Information of Pronto Plus
| Product NDC: | 63736-240 |
| Proprietary Name: | Pronto Plus |
| Non Proprietary Name: | Pyrantel pamoate |
| Active Ingredient(s): | 5 mL/250mL & nbsp; Pyrantel pamoate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pronto Plus
| Product NDC: | 63736-240 |
| Labeler Name: | Insight Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part357B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100920 |
Package Information of Pronto Plus
| Package NDC: | 63736-240-24 |
| Package Description: | 24 CARTON in 1 CASE (63736-240-24) > 1 BOTTLE in 1 CARTON > 59 mL in 1 BOTTLE |
NDC Information of Pronto Plus
| NDC Code | 63736-240-24 |
| Proprietary Name | Pronto Plus |
| Package Description | 24 CARTON in 1 CASE (63736-240-24) > 1 BOTTLE in 1 CARTON > 59 mL in 1 BOTTLE |
| Product NDC | 63736-240 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pyrantel pamoate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100920 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals LLC |
| Substance Name | PYRANTEL PAMOATE |
| Strength Number | 5 |
| Strength Unit | mL/250mL |
| Pharmaceutical Classes |
