Gabapentin

Product NDC
55700-686
11-digit product format
557000686
Labeler code
55700
Product ID
55700-686_503fffe2-3a5a-4a34-8728-e0cc9f5b6c8b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA205101
Marketing category
ANDA
Marketing start
2018-09-21
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-686-30EA - Each55700-6860f08d718-416f-4745-9549-a5aa62ed60b212018-10-11
55700-686-60EA - Each55700-68654a34c06-9a65-4646-bf12-fee75c6556be12018-10-11
55700-686-90EA - Each55700-686fff7f5c1-00e8-4f1b-9128-2547b325337d12018-10-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55700-686-305570006863030 TABLET in 1 BOTTLE (55700-686-30) 30 tablet2018-09-210000-00-00NoNoCurrent
55700-686-605570006866060 TABLET in 1 BOTTLE (55700-686-60) 60 tablet2018-09-210000-00-00NoNoCurrent