Gabapentin

Product NDC
63739-560
11-digit product format
637390560
Labeler code
63739
Product ID
63739-560_b8cc1dc9-73a1-9ea3-e053-2a95a90ae9a6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA078926
Marketing category
ANDA
Marketing start
2012-10-16
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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-560-102020-07-22C16284748780-1ab0e2407-35b7-f274-e053-dbdaa90a6471fbcc94fb-5a74-4aec-b3c0-c3b70f750dd3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-560-10EA - Each63739-56062f2ada0-32ba-4f70-915c-7d92b2472b1c12015-07-20

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63739-560GABAPENTIN TABLET, FILM COATED [MCKESSON CORPORATION DBA SKY PACKAGING]13Legacy NDC20241222_fbcc94fb-5a74-4aec-b3c0-c3b70f750dd3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63739-560-106373905601010 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-560-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK10 blister pack2015-07-060000-00-00NoNoCurrent