| Product NDC: | 13893-689 |
| Proprietary Name: | Pin X |
| Non Proprietary Name: | pyrantel pamoate |
| Active Ingredient(s): | 720.5 mg/1 & nbsp; pyrantel pamoate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 13893-689 |
| Labeler Name: | Quartz Specialty Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part357B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111031 |
| Package NDC: | 13893-689-08 |
| Package Description: | 12 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (13893-689-08) |
| NDC Code | 13893-689-08 |
| Proprietary Name | Pin X |
| Package Description | 12 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (13893-689-08) |
| Product NDC | 13893-689 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pyrantel pamoate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20111031 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Quartz Specialty Pharmaceuticals, LLC |
| Substance Name | PYRANTEL PAMOATE |
| Strength Number | 720.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |