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"53002-2199-3" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE (53002-2199-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-2199-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (53002-2199-3)
Product NDC53002-2199
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20151222
Marketing Category NameANDA
Application NumberANDA206530
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/53002-2199-3





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