Product NDC: | 64092-031 |
Proprietary Name: | Childrens Pain Relief |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 80 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64092-031 |
Labeler Name: | GREAT LAKES WHOLESALE, MARKETING, & SALES, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20050203 |
Package NDC: | 64092-031-20 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (64092-031-20) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC |
NDC Code | 64092-031-20 |
Proprietary Name | Childrens Pain Relief |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (64092-031-20) > 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC |
Product NDC | 64092-031 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20050203 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | GREAT LAKES WHOLESALE, MARKETING, & SALES, INC. |
Substance Name | ACETAMINOPHEN |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes |