"64679-742-01" National Drug Code (NDC)

Ranitidine 30 TABLET in 1 BOTTLE (64679-742-01)
(Wockhardt USA LLC.)

NDC Code64679-742-01
Package Description30 TABLET in 1 BOTTLE (64679-742-01)
Product NDC64679-742
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20091211
Marketing Category NameANDA
Application NumberANDA078701
ManufacturerWockhardt USA LLC.
Substance NameRANITIDINE HYDROCHLORIDE
Strength300
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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