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"0378-3020-05" National Drug Code (NDC)

Famotidine 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3020-05)
(Mylan Pharmaceuticals Inc.)

NDC Code0378-3020-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3020-05)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0378-3020-05





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