daytime pe - 56062-215-53 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of daytime pe

Product NDC: 56062-215
Proprietary Name: daytime pe
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of daytime pe

Product NDC: 56062-215
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19960222

Package Information of daytime pe

Package NDC: 56062-215-53
Package Description: 1 BLISTER PACK in 1 CARTON (56062-215-53) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of daytime pe

NDC Code 56062-215-53
Proprietary Name daytime pe
Package Description 1 BLISTER PACK in 1 CARTON (56062-215-53) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 56062-215
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 19960222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Publix Super Markets Inc
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of daytime pe


General Information