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"72789-177-82" National Drug Code (NDC)

Primidone 500 TABLET in 1 BOTTLE, PLASTIC (72789-177-82)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-177-82
Package Description500 TABLET in 1 BOTTLE, PLASTIC (72789-177-82)
Product NDC72789-177
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrimidone
Non-Proprietary NamePrimidone
Dosage FormTABLET
UsageORAL
Start Marketing Date20210222
Marketing Category NameANDA
Application NumberANDA040586
ManufacturerPD-Rx Pharmaceuticals, Inc.
Substance NamePRIMIDONE
Strength250
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72789-177-82





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