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"69097-811-12" National Drug Code (NDC)

Gabapentin 500 TABLET in 1 BOTTLE (69097-811-12)
(Cipla USA Inc.)

NDC Code69097-811-12
Package Description500 TABLET in 1 BOTTLE (69097-811-12)
Product NDC69097-811
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGabapentin
Non-Proprietary NameGabapentin
Dosage FormTABLET
UsageORAL
Start Marketing Date20160722
Marketing Category NameANDA
Application NumberANDA202764
ManufacturerCipla USA Inc.
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/69097-811-12





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