Gabapentin

Product NDC
72162-1813
11-digit product format
721621813
Labeler code
72162
Product ID
72162-1813_e8a268d7-a080-4540-8ac9-63201fd965e4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078428
Marketing category
ANDA
Marketing start
2009-11-24
Substance
GABAPENTIN
Active strength
300 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
72162-1813-172162181301100 CAPSULE in 1 BOTTLE (72162-1813-1) 100 capsule2024-11-01NoNoHistorical
72162-1813-272162181302120 CAPSULE in 1 BOTTLE (72162-1813-2) 120 capsule2024-11-01NoNoHistorical
72162-1813-47216218130420 CAPSULE in 1 BOTTLE (72162-1813-4) 20 capsule2024-11-01NoNoHistorical
72162-1813-67216218130660 CAPSULE in 1 BOTTLE (72162-1813-6) 60 capsule2024-11-01NoNoHistorical
72162-1813-772162181307180 CAPSULE in 1 BOTTLE (72162-1813-7) 180 capsule2024-11-01NoNoHistorical
72162-1813-87216218130884 CAPSULE in 1 BOTTLE (72162-1813-8) 84 capsule2024-11-01NoNoHistorical
72162-1813-97216218130990 CAPSULE in 1 BOTTLE (72162-1813-9) 90 capsule2024-11-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GabapentinBryant Ranch Prepack2024-11-01HUMAN PRESCRIPTION DRUG LABEL103