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"63868-667-15" National Drug Code (NDC)
Allergy Relief 3 BLISTER PACK in 1 CARTON (63868-667-15) > 5 TABLET in 1 BLISTER PACK
(CHAIN DRUG MARKETING ASSOCIATION INC.)
NDC Code
63868-667-15
Package Description
3 BLISTER PACK in 1 CARTON (63868-667-15) > 5 TABLET in 1 BLISTER PACK
Product NDC
63868-667
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Allergy Relief
Non-Proprietary Name
Fexofenadine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20180901
End Marketing Date
20230228
Marketing Category Name
ANDA
Application Number
ANDA204507
Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC.
Substance Name
FEXOFENADINE HYDROCHLORIDE
Strength
180
Strength Unit
mg/1
Pharmacy Classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63868-667-15