Gabapentin

Product NDC
60687-591
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
American Health Packaging
Application
ANDA090858
Marketing category
ANDA
Substance
GABAPENTIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60687-591-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-591-01) / 1 CAPSULE in 1 BLISTER PACK (60687-591-11) 20210106NoHistorical

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
bbfdedd7-2baf-4bc6-be59-548a5cf21752These 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: 1993American Health Packaging2025-10-03HUMAN PRESCRIPTION DRUG LABEL7
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