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"67296-2330-2" National Drug Code (NDC)

Famotidine 20 TABLET, FILM COATED in 1 BOTTLE (67296-2330-2)
(Redpharm Drug)

NDC Code67296-2330-2
Package Description20 TABLET, FILM COATED in 1 BOTTLE (67296-2330-2)
Product NDC67296-2330
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211104
Marketing Category NameANDA
Application NumberANDA215767
ManufacturerRedpharm Drug
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/67296-2330-2





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