Product NDC: | 47682-102 |
Proprietary Name: | Medique Onset Forte |
Non Proprietary Name: | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE AND PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 162.5; 2; 5 mg/1; mg/1; mg/1 & nbsp; ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE AND PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47682-102 |
Labeler Name: | Unifirst First Aid Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20081230 |
Package NDC: | 47682-102-64 |
Package Description: | 12 PACKET in 1 BOX, UNIT-DOSE (47682-102-64) > 2 TABLET, FILM COATED in 1 PACKET (47682-102-99) |
NDC Code | 47682-102-64 |
Proprietary Name | Medique Onset Forte |
Package Description | 12 PACKET in 1 BOX, UNIT-DOSE (47682-102-64) > 2 TABLET, FILM COATED in 1 PACKET (47682-102-99) |
Product NDC | 47682-102 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE AND PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20081230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Unifirst First Aid Corporation |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 162.5; 2; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |