"55111-220-05" National Drug Code (NDC)

Lamotrigine 500 TABLET in 1 BOTTLE (55111-220-05)
(Dr.Reddy's Laboratories Limited)

NDC Code55111-220-05
Package Description500 TABLET in 1 BOTTLE (55111-220-05)
Product NDC55111-220
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamotrigine
Non-Proprietary NameLamotrigine
Dosage FormTABLET
UsageORAL
Start Marketing Date20090129
Marketing Category NameANDA
Application NumberANDA076708
ManufacturerDr.Reddy's Laboratories Limited
Substance NameLAMOTRIGINE
Strength25
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]

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