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"67877-429-10" National Drug Code (NDC)
Gabapentin 1000 TABLET in 1 BOTTLE (67877-429-10)
(Ascend Laboratories, LLC)
NDC Code
67877-429-10
Package Description
1000 TABLET in 1 BOTTLE (67877-429-10)
Product NDC
67877-429
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20151101
Marketing Category Name
ANDA
Application Number
ANDA206402
Manufacturer
Ascend Laboratories, LLC
Substance Name
GABAPENTIN
Strength
800
Strength Unit
mg/1
Pharmacy Classes
Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67877-429-10