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 |