"49999-043-30" National Drug Code (NDC)

Ranitidine 30 TABLET, FILM COATED in 1 BOTTLE (49999-043-30)
(Quality Care Products, LLC)

NDC Code49999-043-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (49999-043-30)
Product NDC49999-043
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20081119
End Marketing Date20220531
Marketing Category NameANDA
Application NumberANDA078542
ManufacturerQuality Care Products, LLC
Substance NameRANITIDINE HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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