Product NDC: | 57344-125 |
Proprietary Name: | Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride |
Non Proprietary Name: | Acetaminophen, Diphenhydramine Hydrochloride, and Phenylephrine Hydrochloride |
Active Ingredient(s): | 325; 12.5; 5 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine Hydrochloride, and Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57344-125 |
Labeler Name: | AAA Pharmaceutical, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20121222 |
Package NDC: | 57344-125-03 |
Package Description: | 4 BLISTER PACK in 1 CARTON (57344-125-03) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 57344-125-03 |
Proprietary Name | Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride |
Package Description | 4 BLISTER PACK in 1 CARTON (57344-125-03) > 12 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 57344-125 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Diphenhydramine Hydrochloride, and Phenylephrine Hydrochloride |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20121222 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | AAA Pharmaceutical, Inc. |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 12.5; 5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |