"58118-1123-8" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BLISTER PACK (58118-1123-8)
(Clinical Solutions Wholesale, LLC)

NDC Code58118-1123-8
Package Description30 TABLET in 1 BLISTER PACK (58118-1123-8)
Product NDC58118-1123
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerClinical Solutions Wholesale, LLC
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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