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"51660-998-30" National Drug Code (NDC)
Fexofenadine Hydrochloride 1 BOTTLE in 1 CARTON (51660-998-30) > 30 TABLET, FILM COATED in 1 BOTTLE
(OHM LABORATORIES INC.)
NDC Code
51660-998-30
Package Description
1 BOTTLE in 1 CARTON (51660-998-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC
51660-998
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Fexofenadine Hydrochloride
Non-Proprietary Name
Fexofenadine Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20220429
Marketing Category Name
ANDA
Application Number
ANDA091567
Manufacturer
OHM LABORATORIES 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/51660-998-30