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"53002-1199-2" National Drug Code (NDC)

Famotidine 20 TABLET in 1 BOTTLE (53002-1199-2)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1199-2
Package Description20 TABLET in 1 BOTTLE (53002-1199-2)
Product NDC53002-1199
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerRPK Pharmaceuticals, Inc.
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/53002-1199-2





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