Gabapentin

Product NDC
71335-2773
11-digit product format
713352773
Labeler code
71335
Product ID
71335-2773_856b5455-cefb-49f0-ab52-3688e4f743e5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078787
Marketing category
ANDA
Marketing start
2008-01-31
Substance
GABAPENTIN
Active strength
400 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
6CW7F3G59XGABAPENTIN60142-96-3GABAPENTIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2773-17133527730190 CAPSULE in 1 BOTTLE (71335-2773-1) 90 capsule2025-10-13NoNoHistorical
71335-2773-27133527730228 CAPSULE in 1 BOTTLE (71335-2773-2) 28 capsule2025-10-13NoNoHistorical
71335-2773-371335277303120 CAPSULE in 1 BOTTLE (71335-2773-3) 120 capsule2025-10-13NoNoHistorical
71335-2773-47133527730430 CAPSULE in 1 BOTTLE (71335-2773-4) 30 capsule2025-10-13NoNoHistorical
71335-2773-57133527730560 CAPSULE in 1 BOTTLE (71335-2773-5) 60 capsule2025-10-13NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GabapentinBryant Ranch Prepack2025-10-13HUMAN PRESCRIPTION DRUG LABEL1