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"51660-035-31" National Drug Code (NDC)

Famotidine 1 BLISTER PACK in 1 CARTON (51660-035-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
(Ohm Laboratories Inc.)

NDC Code51660-035-31
Package Description1 BLISTER PACK in 1 CARTON (51660-035-31) > 30 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC51660-035
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100215
Marketing Category NameANDA
Application NumberANDA090283
ManufacturerOhm Laboratories Inc.
Substance NameFAMOTIDINE
Strength10
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51660-035-31





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