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"0615-8021-39" National Drug Code (NDC)

Ranitidine 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8021-39)
(NCS HealthCare of KY, LLC dba Vangard Labs)

NDC Code0615-8021-39
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8021-39)
Product NDC0615-8021
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20081119
End Marketing Date20210430
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
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/0615-8021-39





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