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"69367-135-06" National Drug Code (NDC)

Gabapentin 500 TABLET in 1 BOTTLE (69367-135-06)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-135-06
Package Description500 TABLET in 1 BOTTLE (69367-135-06)
Product NDC69367-135
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
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/69367-135-06





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