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"72789-331-30" National Drug Code (NDC)

Famotidine 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-30)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-331-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-331-30)
Product NDC72789-331
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211104
Marketing Category NameANDA
Application NumberANDA215767
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/72789-331-30





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