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"10202-229-66" National Drug Code (NDC)

Fexofenadine Hydrochloride 1 BLISTER PACK in 1 CARTON (10202-229-66) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(7-eleven)

NDC Code10202-229-66
Package Description1 BLISTER PACK in 1 CARTON (10202-229-66) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC10202-229
Product Type NameHUMAN OTC DRUG
Proprietary NameFexofenadine Hydrochloride
Non-Proprietary NameFexofenadine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150115
Marketing Category NameANDA
Application NumberANDA202039
Manufacturer7-eleven
Substance NameFEXOFENADINE HYDROCHLORIDE
Strength180
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/10202-229-66





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