Product NDC: | 68788-9837 |
Proprietary Name: | Childrens QPAP |
Non Proprietary Name: | acetaminophen |
Active Ingredient(s): | 160 mg/5mL & nbsp; acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9837 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120329 |
Package NDC: | 68788-9837-1 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (68788-9837-1) |
NDC Code | 68788-9837-1 |
Proprietary Name | Childrens QPAP |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (68788-9837-1) |
Product NDC | 68788-9837 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20120329 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | ACETAMINOPHEN |
Strength Number | 160 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |