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Nighttime Sinus - 68016-201-16 - (Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride)

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Drug Information of Nighttime Sinus

Product NDC: 68016-201
Proprietary Name: Nighttime Sinus
Non Proprietary Name: Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 6.25; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Nighttime Sinus

Product NDC: 68016-201
Labeler Name: Chain Drug Consortium, LLC (Premier Value)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121018

Package Information of Nighttime Sinus

Package NDC: 68016-201-16
Package Description: 2 BLISTER PACK in 1 CARTON (68016-201-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Nighttime Sinus

NDC Code 68016-201-16
Proprietary Name Nighttime Sinus
Package Description 2 BLISTER PACK in 1 CARTON (68016-201-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 68016-201
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20121018
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Chain Drug Consortium, LLC (Premier Value)
Substance Name ACETAMINOPHEN; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 6.25; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Nighttime Sinus


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