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"52125-136-02" National Drug Code (NDC)

Ranitidine 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-136-02)
(REMEDYREPACK INC.)

NDC Code52125-136-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (52125-136-02)
Product NDC52125-136
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130326
Marketing Category NameANDA
Application NumberANDA075165
ManufacturerREMEDYREPACK INC.
Substance NameRANITIDINE HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-136-02





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