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"58602-733-03" National Drug Code (NDC)

Ranitidine 1 BLISTER PACK in 1 CARTON (58602-733-03) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Aurohealth LLC)

NDC Code58602-733-03
Package Description1 BLISTER PACK in 1 CARTON (58602-733-03) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC58602-733
Product Type NameHUMAN OTC DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171113
Marketing Category NameANDA
Application NumberANDA207579
ManufacturerAurohealth LLC
Substance NameRANITIDINE HYDROCHLORIDE
Strength75
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58602-733-03





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