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"68071-2190-3" National Drug Code (NDC)

Ranitidine 30 TABLET in 1 BOTTLE (68071-2190-3)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-2190-3
Package Description30 TABLET in 1 BOTTLE (68071-2190-3)
Product NDC68071-2190
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20091216
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerNuCare Pharmaceuticals, 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/68071-2190-3





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