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"21130-571-22" National Drug Code (NDC)

Fexofenadine Hydrochloride 3 BLISTER PACK in 1 CARTON (21130-571-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK
(Safeway)

NDC Code21130-571-22
Package Description3 BLISTER PACK in 1 CARTON (21130-571-22) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC21130-571
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110415
Marketing Category NameANDA
Application NumberANDA076447
ManufacturerSafeway
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/21130-571-22





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