"64679-742-03" National Drug Code (NDC)

Ranitidine 10 BLISTER PACK in 1 CARTON (64679-742-03) > 10 TABLET in 1 BLISTER PACK
(Wockhardt USA LLC.)

NDC Code64679-742-03
Package Description10 BLISTER PACK in 1 CARTON (64679-742-03) > 10 TABLET in 1 BLISTER PACK
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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