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"49349-577-02" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-577-02)
(REMEDYREPACK INC.)

NDC Code49349-577-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-577-02)
Product NDC49349-577
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130305
Marketing Category NameANDA
Application NumberANDA075786
ManufacturerREMEDYREPACK 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/49349-577-02





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