Gabapentin

Product NDC
49999-784
11-digit product format
499990784
Labeler code
49999
Product ID
49999-784_e6831ceb-ebac-4b12-aef4-32876b2e38ac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medica & Surgical Supply DBA Quality Care Products LLC
Application
ANDA077662
Marketing category
ANDA
Marketing start
2011-11-04
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
600 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
49999-784-30EA - Each49999-784f64a8492-162f-4703-bcd2-6b9253cf2daa12012-07-24
49999-784-60EA - Each49999-78470e563a4-d4aa-4d73-bb3c-1cf572b0aa5b12012-07-24
49999-784-90EA - Each49999-784c5f53b84-e3dd-497a-8327-15db722909a812012-07-24