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"68382-205-10" National Drug Code (NDC)
Gabapentin 1000 TABLET, FILM COATED in 1 BOTTLE (68382-205-10)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
68382-205-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (68382-205-10)
Product NDC
68382-205
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20121016
Marketing Category Name
ANDA
Application Number
ANDA078926
Manufacturer
Zydus Pharmaceuticals USA Inc.
Substance Name
GABAPENTIN
Strength
800
Strength Unit
mg/1
Pharmacy Classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-205-10