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"37808-571-22" National Drug Code (NDC)
Allergy Relief 15 BLISTER PACK in 1 CARTON (37808-571-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK
(H E B)
NDC Code
37808-571-22
Package Description
15 BLISTER PACK in 1 CARTON (37808-571-22) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC
37808-571
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Allergy Relief
Non-Proprietary Name
Fexofenadine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110622
Marketing Category Name
ANDA
Application Number
ANDA076447
Manufacturer
H E B
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/37808-571-22