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"53002-6672-2" National Drug Code (NDC)

Famotidine 20 TABLET in 1 BOTTLE (53002-6672-2)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-6672-2
Package Description20 TABLET in 1 BOTTLE (53002-6672-2)
Product NDC53002-6672
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerRPK Pharmaceuticals, Inc.
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/53002-6672-2





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