"55111-131-81" National Drug Code (NDC)

Ranitidine 3 BLISTER PACK in 1 CARTON (55111-131-81) > 10 TABLET in 1 BLISTER PACK
(Dr. Reddy's Laboratories Limited)

NDC Code55111-131-81
Package Description3 BLISTER PACK in 1 CARTON (55111-131-81) > 10 TABLET in 1 BLISTER PACK
Product NDC55111-131
Product Type NameHUMAN OTC DRUG
Proprietary NameRanitidine
Non-Proprietary NameRanitidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20000301
Marketing Category NameANDA
Application NumberANDA075294
ManufacturerDr. Reddy's Laboratories Limited
Substance NameRANITIDINE HYDROCHLORIDE
Strength75
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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