| Product NDC: | 13893-691 |
| Proprietary Name: | Pin-X |
| Non Proprietary Name: | pyrantel pamoate |
| Active Ingredient(s): | 144 mg/mL & nbsp; pyrantel pamoate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 13893-691 |
| Labeler Name: | Quartz Specialty Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part357B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20010901 |
| Package NDC: | 13893-691-45 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (13893-691-45) > 30 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 13893-691-45 |
| Proprietary Name | Pin-X |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (13893-691-45) > 30 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 13893-691 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pyrantel pamoate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20010901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Quartz Specialty Pharmaceuticals, LLC |
| Substance Name | PYRANTEL PAMOATE |
| Strength Number | 144 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |