Product NDC: | 42507-476 |
Proprietary Name: | allergy |
Non Proprietary Name: | Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl |
Active Ingredient(s): | 325; 2; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42507-476 |
Labeler Name: | HyVee Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060204 |
Package NDC: | 42507-476-62 |
Package Description: | 2 BLISTER PACK in 1 CARTON (42507-476-62) > 12 TABLET in 1 BLISTER PACK |
NDC Code | 42507-476-62 |
Proprietary Name | allergy |
Package Description | 2 BLISTER PACK in 1 CARTON (42507-476-62) > 12 TABLET in 1 BLISTER PACK |
Product NDC | 42507-476 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20060204 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | HyVee Inc |
Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 2; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |