Product NDC: | 50844-185 |
Proprietary Name: | Childrens Chewable Pain Reliever |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 80 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50844-185 |
Labeler Name: | L.N.K. International, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19900410 |
Package NDC: | 50844-185-08 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50844-185-08) > 24 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC |
NDC Code | 50844-185-08 |
Proprietary Name | Childrens Chewable Pain Reliever |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50844-185-08) > 24 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC |
Product NDC | 50844-185 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 19900410 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | L.N.K. International, Inc. |
Substance Name | ACETAMINOPHEN |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes |