"76420-837-05" National Drug Code (NDC)

Gabapentin 500 TABLET in 1 BOTTLE (76420-837-05)
(Asclemed USA, Inc.)

NDC Code76420-837-05
Package Description500 TABLET in 1 BOTTLE (76420-837-05)
Product NDC76420-837
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20211001
Marketing Category NameANDA
Application NumberANDA214957
ManufacturerAsclemed USA, Inc.
Substance NameGABAPENTIN
Strength800
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]

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