Gabapentin

Product NDC
42708-056
11-digit product format
427080056
Labeler code
42708
Product ID
42708-056_a9179a9a-b5f6-4ac8-931f-49856bc8270a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
QPharma Inc
Application
ANDA090858
Marketing category
ANDA
Marketing start
2016-05-06
Marketing end
0000-00-00
Substance
GABAPENTIN
Active strength
300 mg/1
Pharmacologic classes
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42708-056-602021-03-12C16284748780-1ba0f9c33-48b4-a910-e053-dadaa90a0b855d1d442d-23a1-4bc5-a880-5a21fc6c6a93
42708-056-602021-01-29C16284748780-1ba0f9c33-48b4-a910-e053-dadaa90a0b855d1d442d-23a1-4bc5-a880-5a21fc6c6a93