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"68071-2306-3" National Drug Code (NDC)

Famotidine 30 TABLET in 1 BOTTLE (68071-2306-3)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2306-3
Package Description30 TABLET in 1 BOTTLE (68071-2306-3)
Product NDC68071-2306
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerNuCare Pharmaceuticals,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/68071-2306-3





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