"76420-235-12" National Drug Code (NDC)

Gabapentin 120 TABLET in 1 BOTTLE (76420-235-12)
(Asclemed USA, Inc.)

NDC Code76420-235-12
Package Description120 TABLET in 1 BOTTLE (76420-235-12)
Product NDC76420-235
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160204
Marketing Category NameANDA
Application NumberANDA205101
ManufacturerAsclemed USA, Inc.
Substance NameGABAPENTIN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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