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"37808-458-39" National Drug Code (NDC)

Rx Act All Day Allergy Relief 1 BOTTLE in 1 CARTON (37808-458-39) > 30 TABLET in 1 BOTTLE
(H E B)

NDC Code37808-458-39
Package Description1 BOTTLE in 1 CARTON (37808-458-39) > 30 TABLET in 1 BOTTLE
Product NDC37808-458
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act All Day Allergy Relief
Non-Proprietary NameCetirizine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20080131
Marketing Category NameANDA
Application NumberANDA078336
ManufacturerH E B
Substance NameCETIRIZINE HYDROCHLORIDE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-458-39





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