"69367-134-03" National Drug Code (NDC)

Gabapentin 90 TABLET in 1 BOTTLE (69367-134-03)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-134-03
Package Description90 TABLET in 1 BOTTLE (69367-134-03)
Product NDC69367-134
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160411
Marketing Category NameANDA
Application NumberANDA205101
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameGABAPENTIN
Strength600
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

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