"10135-522-10" National Drug Code (NDC)

Primidone 1000 TABLET in 1 BOTTLE (10135-522-10)
(Marlex Pharmaceuticals Inc)

NDC Code10135-522-10
Package Description1000 TABLET in 1 BOTTLE (10135-522-10)
Product NDC10135-522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrimidone
Non-Proprietary NamePrimidone
Dosage FormTABLET
UsageORAL
Start Marketing Date20150501
Marketing Category NameANDA
Application NumberANDA084903
ManufacturerMarlex Pharmaceuticals Inc
Substance NamePRIMIDONE
Strength250
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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