"43063-695-90" National Drug Code (NDC)

Famotidine 90 TABLET in 1 BOTTLE, PLASTIC (43063-695-90)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code43063-695-90
Package Description90 TABLET in 1 BOTTLE, PLASTIC (43063-695-90)
Product NDC43063-695
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFamotidine
Non-Proprietary NameFamotidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20010416
Marketing Category NameANDA
Application NumberANDA075805
ManufacturerPD-Rx Pharmaceuticals, Inc.
Substance NameFAMOTIDINE
Strength20
Strength Unitmg/1
Pharmacy ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]

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