"62332-002-71" National Drug Code (NDC)

Famotidine 500 TABLET in 1 BOTTLE (62332-002-71)
(Alembic Pharmaceuticals Inc.)

NDC Code62332-002-71
Package Description500 TABLET in 1 BOTTLE (62332-002-71)
Product NDC62332-002
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20160129
Marketing Category NameANDA
Application NumberANDA078916
ManufacturerAlembic Pharmaceuticals Inc.
Substance NameFAMOTIDINE
Strength40
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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