"0093-0039-05" National Drug Code (NDC)

Lamotrigine 500 TABLET in 1 BOTTLE (0093-0039-05)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0039-05
Package Description500 TABLET in 1 BOTTLE (0093-0039-05)
Product NDC0093-0039
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamotrigine
Non-Proprietary NameLamotrigine
Dosage FormTABLET
UsageORAL
Start Marketing Date20080722
Marketing Category NameANDA
Application NumberANDA076388
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameLAMOTRIGINE
Strength25
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0039-05