Gabapentin

Product NDC
63629-7305
11-digit product format
636297305
Labeler code
63629
Product ID
63629-7305_ae508b2a-2235-48e1-8fd3-8e580091f70f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075350
Marketing category
ANDA
Marketing start
2014-04-23
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
100 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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-7305-1EA - Each63629-7305f26fe4e6-6b39-4b82-a820-b3bb5c775aba12019-05-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-7305-16362973050190 CAPSULE in 1 BOTTLE (63629-7305-1) 90 capsule2017-09-140000-00-00NoNoCurrent
63629-7305-26362973050228 CAPSULE in 1 BOTTLE (63629-7305-2) 28 capsule2017-09-140000-00-00NoNoCurrent
63629-7305-36362973050330 CAPSULE in 1 BOTTLE (63629-7305-3) 30 capsule2017-09-140000-00-00NoNoCurrent
63629-7305-46362973050460 CAPSULE in 1 BOTTLE (63629-7305-4) 60 capsule2017-09-140000-00-00NoNoCurrent
63629-7305-563629730505120 CAPSULE in 1 BOTTLE (63629-7305-5) 120 capsule2017-09-140000-00-00NoNoCurrent
63629-7305-66362973050684 CAPSULE in 1 BOTTLE (63629-7305-6) 84 capsule2017-09-140000-00-00NoNoCurrent