Gabapentin

Product NDC
55154-8194
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Cardinal Health 107, LLC
Application
ANDA090858
Marketing category
ANDA
Substance
GABAPENTIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55154-8194-010 BLISTER PACK in 1 BAG (55154-8194-0) / 1 CAPSULE in 1 BLISTER PACK20201125NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
d4f21e97-5e55-44c9-9b31-5f79ac2eb512These highlights do not include all the information needed to use GABAPENTIN CAPSULES safely and effectively. See full prescribing information for GABAPENTIN CAPSULES. GABAPENTIN capsules, for oral use Initial U.S. Approval: 1993Cardinal Health 107, LLC2026-01-12HUMAN PRESCRIPTION DRUG LABEL5
d4f21e97-5e55-44c9-9b31-5f79ac2eb512These highlights do not include all the information needed to use GABAPENTIN CAPSULES safely and effectively. See full prescribing information for GABAPENTIN CAPSULES. GABAPENTIN capsules, for oral use Initial U.S. Approval: 1993Cardinal Health 107, LLC2024-07-31HUMAN PRESCRIPTION DRUG LABEL3