"68382-607-05" National Drug Code (NDC)

Gabapentin 500 TABLET in 1 BOTTLE (68382-607-05)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-607-05
Package Description500 TABLET in 1 BOTTLE (68382-607-05)
Product NDC68382-607
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20240125
Marketing Category NameANDA
Application NumberANDA203934
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameGABAPENTIN
Strength600
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]

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