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"71335-2037-9" National Drug Code (NDC)

Gabapentin 135 TABLET in 1 BOTTLE (71335-2037-9)
(Bryant Ranch Prepack)

NDC Code71335-2037-9
Package Description135 TABLET in 1 BOTTLE (71335-2037-9)
Product NDC71335-2037
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20151101
Marketing Category NameANDA
Application NumberANDA206402
ManufacturerBryant Ranch Prepack
Substance NameGABAPENTIN
Strength800
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2037-9





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