Product NDC: | 49638-002 |
Proprietary Name: | TYLO |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49638-002 |
Labeler Name: | America Medic |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120515 |
Package NDC: | 49638-002-03 |
Package Description: | 1 BOTTLE in 1 BOX (49638-002-03) > 60 TABLET in 1 BOTTLE (49638-002-02) |
NDC Code | 49638-002-03 |
Proprietary Name | TYLO |
Package Description | 1 BOTTLE in 1 BOX (49638-002-03) > 60 TABLET in 1 BOTTLE (49638-002-02) |
Product NDC | 49638-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120515 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | America Medic |
Substance Name | ACETAMINOPHEN |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |