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"70934-199-30" National Drug Code (NDC)

Cetirizine Hydrochloride 30 TABLET in 1 BOTTLE, PLASTIC (70934-199-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-199-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70934-199-30)
Product NDC70934-199
Product Type NameHUMAN OTC DRUG
Proprietary NameCetirizine Hydrochloride
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20181204
End Marketing Date20240930
Marketing Category NameANDA
Application NumberANDA077829
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
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/70934-199-30





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