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"52125-808-02" National Drug Code (NDC)
Gabapentin 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-808-02)
(REMEDYREPACK INC.)
NDC Code
52125-808-02
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (52125-808-02)
Product NDC
52125-808
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gabapentin
Non-Proprietary Name
Gabapentin
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140109
Marketing Category Name
ANDA
Application Number
ANDA200651
Manufacturer
REMEDYREPACK 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/52125-808-02