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"37808-194-71" National Drug Code (NDC)

Rx Act Heartburn Prevention 1 BOTTLE in 1 CARTON (37808-194-71) > 50 TABLET in 1 BOTTLE
(H E B)

NDC Code37808-194-71
Package Description1 BOTTLE in 1 CARTON (37808-194-71) > 50 TABLET in 1 BOTTLE
Product NDC37808-194
Product Type NameHUMAN OTC DRUG
Proprietary NameRx Act Heartburn Prevention
Proprietary Name SuffixMaximum Strength
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20060928
Marketing Category NameANDA
Application NumberANDA077351
ManufacturerH E B
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37808-194-71





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