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"25000-087-36" National Drug Code (NDC)

Famotidine 20 Mg 3 BLISTER PACK in 1 CARTON (25000-087-36) / 10 TABLET, COATED in 1 BLISTER PACK
(MARKSANS PHARMA LIMITED)

NDC Code25000-087-36
Package Description3 BLISTER PACK in 1 CARTON (25000-087-36) / 10 TABLET, COATED in 1 BLISTER PACK
Product NDC25000-087
Product Type NameHUMAN OTC DRUG
Proprietary NameFamotidine 20 Mg
Non-Proprietary NameFamotidine 20 Mg
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20230310
Marketing Category NameANDA
Application NumberANDA217543
ManufacturerMARKSANS PHARMA LIMITED
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/25000-087-36





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