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"25000-220-81" National Drug Code (NDC)

Cetirizine Hydrochloride Tablets, 10 Mg 1 BLISTER PACK in 1 CARTON (25000-220-81) / 14 TABLET in 1 BLISTER PACK
(MARKSANS PHARMA LIMITED)

NDC Code25000-220-81
Package Description1 BLISTER PACK in 1 CARTON (25000-220-81) / 14 TABLET in 1 BLISTER PACK
Product NDC25000-220
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride Tablets, 10 Mg
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20220113
Marketing Category NameANDA
Application NumberANDA078933
ManufacturerMARKSANS PHARMA LIMITED
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/25000-220-81





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