Product NDC: | 0904-6158 |
Proprietary Name: | infants acetaminophen |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 80 mg/.8mL & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0904-6158 |
Labeler Name: | Major Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101112 |
Package NDC: | 0904-6158-30 |
Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (0904-6158-30) > 30 mL in 1 BOTTLE, DROPPER |
NDC Code | 0904-6158-30 |
Proprietary Name | infants acetaminophen |
Package Description | 1 BOTTLE, DROPPER in 1 CARTON (0904-6158-30) > 30 mL in 1 BOTTLE, DROPPER |
Product NDC | 0904-6158 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | SUSPENSION/ DROPS |
Route Name | ORAL |
Start Marketing Date | 20101112 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Major Pharmaceuticals |
Substance Name | ACETAMINOPHEN |
Strength Number | 80 |
Strength Unit | mg/.8mL |
Pharmaceutical Classes |