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"68001-412-03" National Drug Code (NDC)

Gabapentin 500 TABLET in 1 BOTTLE (68001-412-03)
(BluePoint Laboratories)

NDC Code68001-412-03
Package Description500 TABLET in 1 BOTTLE (68001-412-03)
Product NDC68001-412
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20190930
Marketing Category NameANDA
Application NumberANDA077662
ManufacturerBluePoint Laboratories
Substance NameGABAPENTIN
Strength800
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/68001-412-03





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