GABAPENTIN

Product NDC
71335-2005
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090007
Marketing category
ANDA
Substance
GABAPENTIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71335-2005-190 CAPSULE in 1 BOTTLE (71335-2005-1) 2021-12-08NoHistorical
71335-2005-228 CAPSULE in 1 BOTTLE (71335-2005-2) 2024-10-31NoHistorical
71335-2005-330 CAPSULE in 1 BOTTLE (71335-2005-3) 2022-01-04NoHistorical
71335-2005-460 CAPSULE in 1 BOTTLE (71335-2005-4) 2024-10-31NoHistorical
71335-2005-5120 CAPSULE in 1 BOTTLE (71335-2005-5) 2024-10-31NoHistorical
71335-2005-684 CAPSULE in 1 BOTTLE (71335-2005-6) 2021-12-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GABAPENTINBryant Ranch Prepack2024-10-31HUMAN PRESCRIPTION DRUG LABEL103