Gabapentin

Product NDC
49999-799
11-digit product format
499990799
Labeler code
49999
Product ID
49999-799_77f1cb91-9dab-4546-a229-1b1b1b4194eb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Quality Care Products, LLC
Application
ANDA077662
Marketing category
ANDA
Marketing start
2010-12-06
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
800 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49999-799-30EA - Each49999-79934f5c985-75c5-4342-8660-5b9731b48d2112012-07-24
49999-799-60EA - Each49999-799db607047-34b4-47f2-a921-4e91385ffeb812012-07-24
49999-799-90EA - Each49999-7991cdefad3-69f1-4a2a-90c8-9213c066823f12012-07-24