Product NDC: | 51645-711 |
Proprietary Name: | Childrens Chewable Acetaminophen |
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: | 51645-711 |
Labeler Name: | Gemini Pharmaceuticals, Inc. dba Plus Pharma |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101203 |
Package NDC: | 51645-711-30 |
Package Description: | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (51645-711-30) |
NDC Code | 51645-711-30 |
Proprietary Name | Childrens Chewable Acetaminophen |
Package Description | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (51645-711-30) |
Product NDC | 51645-711 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20101203 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Gemini Pharmaceuticals, Inc. dba Plus Pharma |
Substance Name | ACETAMINOPHEN |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes |