Gabapentin

Product NDC
68788-7614
11-digit product format
687887614
Labeler code
68788
Product ID
68788-7614_eec606e5-ef7b-4c42-ba5b-7d7194c1b526
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA206943
Marketing category
ANDA
Marketing start
2020-02-07
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
400 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7614-168788761401100 CAPSULE in 1 BOTTLE, PLASTIC (68788-7614-1) 100 capsule2020-02-070000-00-00NoNoCurrent
68788-7614-36878876140330 CAPSULE in 1 BOTTLE, PLASTIC (68788-7614-3) 30 capsule2020-02-070000-00-00NoNoCurrent
68788-7614-66878876140660 CAPSULE in 1 BOTTLE, PLASTIC (68788-7614-6) 60 capsule2020-02-070000-00-00NoNoCurrent
68788-7614-868788761408120 CAPSULE in 1 BOTTLE, PLASTIC (68788-7614-8) 120 capsule2020-02-070000-00-00NoNoCurrent
68788-7614-96878876140990 CAPSULE in 1 BOTTLE, PLASTIC (68788-7614-9) 90 capsule2020-02-070000-00-00NoNoCurrent