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"68382-205-30" National Drug Code (NDC)
Gabapentin 10 BLISTER PACK in 1 CARTON (68382-205-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Zydus Pharmaceuticals (USA) Inc.)
NDC Code
68382-205-30
Package Description
10 BLISTER PACK in 1 CARTON (68382-205-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK
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
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-205-30