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"49349-254-02" National Drug Code (NDC)

Dilantin 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (49349-254-02)
(REMEDYREPACK INC.)

NDC Code49349-254-02
Package Description30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (49349-254-02)
Product NDC49349-254
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDilantin
Non-Proprietary NameDilantin
Dosage FormCAPSULE, EXTENDED RELEASE
UsageORAL
Start Marketing Date20110505
Marketing Category NameANDA
Application NumberANDA084349
ManufacturerREMEDYREPACK INC.
Substance NamePHENYTOIN SODIUM
Strength30
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/49349-254-02





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