"0378-3020-01" National Drug Code (NDC)

Famotidine 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3020-01)
(Mylan Pharmaceuticals Inc.)

NDC Code0378-3020-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3020-01)
Product NDC0378-3020
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
End Marketing Date20200229
Marketing Category NameANDA
Application NumberANDA075704
ManufacturerMylan Pharmaceuticals Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

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