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"80005-118-14" National Drug Code (NDC)

Primidone 500 TABLET in 1 BOTTLE (80005-118-14)
(Carnegie Pharmaceuticals LLC)

NDC Code80005-118-14
Package Description500 TABLET in 1 BOTTLE (80005-118-14)
Product NDC80005-118
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrimidone
Non-Proprietary NamePrimidone
Dosage FormTABLET
UsageORAL
Start Marketing Date20240501
Marketing Category NameANDA
Application NumberANDA218366
ManufacturerCarnegie Pharmaceuticals LLC
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/80005-118-14





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