"37808-583-39" National Drug Code (NDC)

Allergy Relief 1 BOTTLE in 1 CARTON (37808-583-39) > 30 TABLET, FILM COATED in 1 BOTTLE
(H E B)

NDC Code37808-583-39
Package Description1 BOTTLE in 1 CARTON (37808-583-39) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC37808-583
Product Type NameHUMAN OTC DRUG
Proprietary NameAllergy Relief
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180126
Marketing Category NameANDA
Application NumberANDA078336
ManufacturerH E B
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]

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