Product NDC: | 0924-0123 |
Proprietary Name: | PhysiciansCare Non Aspirin |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0924-0123 |
Labeler Name: | Acme United Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120120 |
Package NDC: | 0924-0123-02 |
Package Description: | 125 PACKET in 1 CARTON (0924-0123-02) > 2 TABLET, FILM COATED in 1 PACKET |
NDC Code | 0924-0123-02 |
Proprietary Name | PhysiciansCare Non Aspirin |
Package Description | 125 PACKET in 1 CARTON (0924-0123-02) > 2 TABLET, FILM COATED in 1 PACKET |
Product NDC | 0924-0123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120120 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Acme United Corporation |
Substance Name | ACETAMINOPHEN |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |