Gabapentin

Product NDC
82804-226
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA075477
Marketing category
ANDA
Substance
GABAPENTIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82804-226-3030 CAPSULE in 1 BOTTLE, PLASTIC (82804-226-30) 2025-05-23NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GabapentinProficient Rx LP2025-05-01HUMAN PRESCRIPTION DRUG LABEL1