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"55111-396-08" National Drug Code (NDC)

Famotidine 1 BLISTER PACK in 1 CARTON (55111-396-08) / 8 TABLET in 1 BLISTER PACK
(Dr.Reddys Laboratories Limited)

NDC Code55111-396-08
Package Description1 BLISTER PACK in 1 CARTON (55111-396-08) / 8 TABLET in 1 BLISTER PACK
Product NDC55111-396
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20060930
Marketing Category NameANDA
Application NumberANDA077367
ManufacturerDr.Reddys Laboratories Limited
Substance NameFAMOTIDINE
Strength20
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/55111-396-08





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