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"70710-1683-1" National Drug Code (NDC)

Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (70710-1683-1)
(Zydus Pharmaceuticals USA Inc.)

NDC Code70710-1683-1
Package Description100 TABLET, FILM COATED in 1 BOTTLE (70710-1683-1)
Product NDC70710-1683
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220606
Marketing Category NameANDA
Application NumberANDA216441
ManufacturerZydus Pharmaceuticals USA Inc.
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/70710-1683-1





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