"37808-302-06" National Drug Code (NDC)

Ranitidine 1 BOTTLE in 1 CARTON (37808-302-06) > 65 TABLET, FILM COATED in 1 BOTTLE
(H-E-B)

NDC Code37808-302-06
Package Description1 BOTTLE in 1 CARTON (37808-302-06) > 65 TABLET, FILM COATED in 1 BOTTLE
Product NDC37808-302
Product Type NameHUMAN OTC DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180124
Marketing Category NameANDA
Application NumberANDA200172
ManufacturerH-E-B
Substance NameRANITIDINE HYDROCHLORIDE
Strength150
Strength Unitmg/1

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