GABAPENTIN

Product NDC
60760-669
11-digit product format
607600669
Labeler code
60760
Product ID
60760-669_336256c3-9dea-89cc-e063-6394a90a42cd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA214956
Marketing category
ANDA
Marketing start
2021-05-10
Substance
GABAPENTIN
Active strength
100 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
60760-669-306076006693030 CAPSULE in 1 BOTTLE, PLASTIC (60760-669-30) 30 capsule2025-04-22NoNoHistorical
60760-669-606076006696060 CAPSULE in 1 BOTTLE, PLASTIC (60760-669-60) 60 capsule2024-09-06NoNoHistorical
60760-669-906076006699090 CAPSULE in 1 BOTTLE, PLASTIC (60760-669-90) 90 capsule2025-02-05NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GABAPENTINST. MARY'S MEDICAL PARK PHARMACY2025-04-22HUMAN PRESCRIPTION DRUG LABEL3