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"72789-027-30" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE, PLASTIC (72789-027-30)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-027-30
Package Description30 TABLET in 1 BOTTLE, PLASTIC (72789-027-30)
Product NDC72789-027
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerPD-Rx 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/72789-027-30





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