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"55111-120-30" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (55111-120-30)
(Dr.Reddy's Laboratories Limited)

NDC Code55111-120-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (55111-120-30)
Product NDC55111-120
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075718
ManufacturerDr.Reddy's Laboratories Limited
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/55111-120-30





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