"70518-1602-0" National Drug Code (NDC)

Lamotrigine 30 TABLET in 1 BLISTER PACK (70518-1602-0)
(REMEDYREPACK INC.)

NDC Code70518-1602-0
Package Description30 TABLET in 1 BLISTER PACK (70518-1602-0)
Product NDC70518-1602
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamotrigine
Non-Proprietary NameLamotrigine
Dosage FormTABLET
UsageORAL
Start Marketing Date20181026
Marketing Category NameANDA
Application NumberANDA077783
ManufacturerREMEDYREPACK INC.
Substance NameLAMOTRIGINE
Strength150
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Anti-epileptic Agent [EPC]

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