GABAPENTIN

Product NDC
60760-605
11-digit product format
607600605
Labeler code
60760
Product ID
60760-605_f06f040b-df23-7087-e053-2995a90ac1e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GABAPENTIN
Dosage form
CAPSULE
Route
ORAL
Labeler
St. Mary
Application
ANDA090007
Marketing category
ANDA
Marketing start
2017-12-26
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60760-605GABAPENTIN CAPSULE [ST. MARY’S MEDICAL PARK PHARMACY]7Legacy NDC20231209_6141b3a6-fcaa-1a06-e053-2991aa0ac7c4.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60760-605-306076006053030 CAPSULE in 1 BOTTLE, PLASTIC (60760-605-30) 30 capsule2018-03-130000-00-00NoNoCurrent
60760-605-606076006056060 CAPSULE in 1 BOTTLE, PLASTIC (60760-605-60) 60 capsule2017-12-290000-00-00NoNoCurrent
60760-605-906076006059090 CAPSULE in 1 BOTTLE, PLASTIC (60760-605-90) 90 capsule2017-12-260000-00-00NoNoCurrent