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"60687-322-01" National Drug Code (NDC)

Ranitidine 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-322-01) > 1 TABLET in 1 BLISTER PACK (60687-322-11)
(American Health Packaging)

NDC Code60687-322-01
Package Description100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-322-01) > 1 TABLET in 1 BLISTER PACK (60687-322-11)
Product NDC60687-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20170818
End Marketing Date20201231
Marketing Category NameANDA
Application NumberANDA077824
ManufacturerAmerican Health Packaging
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/60687-322-01





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