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"68788-7853-4" National Drug Code (NDC)

Famotidine 14 TABLET in 1 BOTTLE (68788-7853-4)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7853-4
Package Description14 TABLET in 1 BOTTLE (68788-7853-4)
Product NDC68788-7853
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20210129
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerPreferred 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/68788-7853-4





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