"21130-191-20" National Drug Code (NDC)

Famotidine 200 TABLET in 1 BOTTLE (21130-191-20)
(SAFEWAY)

NDC Code21130-191-20
Package Description200 TABLET in 1 BOTTLE (21130-191-20)
Product NDC21130-191
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20230630
Marketing Category NameANDA
Application NumberANDA215822
ManufacturerSAFEWAY
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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