GABAPENTIN

Product NDC
68788-7727
11-digit product format
687887727
Labeler code
68788
Product ID
68788-7727_fb08dde1-16fe-442a-be84-715a2306ab30
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GABAPENTIN
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA090007
Marketing category
ANDA
Marketing start
2020-07-01
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7727-168788772701100 CAPSULE in 1 BOTTLE (68788-7727-1) 100 capsule2020-07-010000-00-00NoNoCurrent
68788-7727-36878877270330 CAPSULE in 1 BOTTLE (68788-7727-3) 30 capsule2020-07-010000-00-00NoNoCurrent
68788-7727-66878877270660 CAPSULE in 1 BOTTLE (68788-7727-6) 60 capsule2020-07-010000-00-00NoNoCurrent
68788-7727-868788772708120 CAPSULE in 1 BOTTLE (68788-7727-8) 120 capsule2020-07-010000-00-00NoNoCurrent
68788-7727-96878877270990 CAPSULE in 1 BOTTLE (68788-7727-9) 90 capsule2020-07-010000-00-00NoNoCurrent