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"68788-9220-1" National Drug Code (NDC)

Famotidine 100 TABLET, FILM COATED in 1 BOTTLE (68788-9220-1)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-9220-1
Package Description100 TABLET, FILM COATED in 1 BOTTLE (68788-9220-1)
Product NDC68788-9220
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075718
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/68788-9220-1





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