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"68788-9217-8" National Drug Code (NDC)

Famotidine 120 TABLET in 1 BOTTLE (68788-9217-8)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-9217-8
Package Description120 TABLET in 1 BOTTLE (68788-9217-8)
Product NDC68788-9217
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20150826
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/68788-9217-8





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