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"21130-022-30" National Drug Code (NDC)

Famotidine 1 BOTTLE in 1 CARTON (21130-022-30) / 30 TABLET in 1 BOTTLE
(Albertsons Companies)

NDC Code21130-022-30
Package Description1 BOTTLE in 1 CARTON (21130-022-30) / 30 TABLET in 1 BOTTLE
Product NDC21130-022
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20211101
Marketing Category NameANDA
Application NumberANDA077367
ManufacturerAlbertsons Companies
Substance NameFAMOTIDINE
Strength10
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/21130-022-30





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