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"69367-401-10" National Drug Code (NDC)

Famotidine 1000 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-401-10)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-401-10
Package Description1000 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-401-10)
Product NDC69367-401
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20240909
Marketing Category NameANDA
Application NumberANDA217669
ManufacturerWestminster Pharmaceuticals, LLC
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/69367-401-10





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