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"71335-1012-7" National Drug Code (NDC)

Gabapentin 500 TABLET, FILM COATED in 1 BOTTLE (71335-1012-7)
(Bryant Ranch Prepack)

NDC Code71335-1012-7
Package Description500 TABLET, FILM COATED in 1 BOTTLE (71335-1012-7)
Product NDC71335-1012
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060824
Marketing Category NameANDA
Application NumberANDA077525
ManufacturerBryant Ranch Prepack
Substance NameGABAPENTIN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1012-7





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