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"61919-200-30" National Drug Code (NDC)

Ranitidine Hydrochloride 30 TABLET in 1 BOTTLE (61919-200-30)
(Direct Rx)

NDC Code61919-200-30
Package Description30 TABLET in 1 BOTTLE (61919-200-30)
Product NDC61919-200
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine Hydrochloride
Non-Proprietary NameRanitidine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerDirect Rx
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/61919-200-30





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