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"61919-102-72" National Drug Code (NDC)

Gabapentin 120 BOTTLE in 1 BOTTLE (61919-102-72) > 90 BOTTLE in 1 BOTTLE (61919-102-90) > 60 BOTTLE in 1 BOTTLE (61919-102-60) > 30 CAPSULE in 1 BOTTLE (61919-102-30)
(Direct Rx)

NDC Code61919-102-72
Package Description120 BOTTLE in 1 BOTTLE (61919-102-72) > 90 BOTTLE in 1 BOTTLE (61919-102-90) > 60 BOTTLE in 1 BOTTLE (61919-102-60) > 30 CAPSULE in 1 BOTTLE (61919-102-30)
Product NDC61919-102
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20150101
Marketing Category NameANDA
Application NumberANDA077242
ManufacturerDirect Rx
Substance NameGABAPENTIN
Strength300
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

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