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"55315-352-31" National Drug Code (NDC)

Ranitidine 1 BLISTER PACK in 1 CARTON (55315-352-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
(Fred's Inc.)

NDC Code55315-352-31
Package Description1 BLISTER PACK in 1 CARTON (55315-352-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC55315-352
Product Type NameHUMAN OTC DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130901
Marketing Category NameANDA
Application NumberANDA201745
ManufacturerFred's Inc.
Substance NameRANITIDINE HYDROCHLORIDE
Strength75
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/55315-352-31





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