"55910-035-08" National Drug Code (NDC)

NDC Code	55910-035-08
Package Description	2 BLISTER PACK in 1 CARTON (55910-035-08) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	55910-035
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cold Multi-symptom Severe
Proprietary Name Suffix	Day Time
Non-Proprietary Name	Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20050804
End Marketing Date	20231209
Marketing Category Name	OTC MONOGRAPH FINAL
Application Number	part341
Manufacturer	DOLGENCORP, LLC
Substance Name	ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength	325; 10; 200; 5
Strength Unit	mg/1; mg/1; mg/1; mg/1