Gabapentin

Product NDC
50090-7672
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA204989
Marketing category
ANDA
Substance
GABAPENTIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7672-030 CAPSULE in 1 BOTTLE (50090-7672-0) 2025-10-08NoHistorical
50090-7672-1100 CAPSULE in 1 BOTTLE (50090-7672-1) 2025-10-08NoHistorical
50090-7672-290 CAPSULE in 1 BOTTLE (50090-7672-2) 2025-10-08NoHistorical
50090-7672-342 CAPSULE in 1 BOTTLE (50090-7672-3) 2025-10-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GabapentinA-S Medication Solutions2025-10-10HUMAN PRESCRIPTION DRUG LABEL1