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"25000-220-08" National Drug Code (NDC)
Cetirizine Hydrochloride Tablets, 10 Mg 1 BOTTLE in 1 CARTON (25000-220-08) / 100 TABLET in 1 BOTTLE
(MARKSANS PHARMA LIMITED)
NDC Code
25000-220-08
Package Description
1 BOTTLE in 1 CARTON (25000-220-08) / 100 TABLET in 1 BOTTLE
Product NDC
25000-220
Product Type Name
HUMAN OTC DRUG
Proprietary Name
Cetirizine Hydrochloride Tablets, 10 Mg
Non-Proprietary Name
Cetirizine Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20220113
Marketing Category Name
ANDA
Application Number
ANDA078933
Manufacturer
MARKSANS PHARMA LIMITED
Substance Name
CETIRIZINE HYDROCHLORIDE
Strength
10
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/25000-220-08