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"42708-049-30" National Drug Code (NDC)

Ranitidine 30 TABLET in 1 BOTTLE (42708-049-30)
(QPharma Inc)

NDC Code42708-049-30
Package Description30 TABLET in 1 BOTTLE (42708-049-30)
Product NDC42708-049
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20091216
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerQPharma 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/42708-049-30





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