Gabapentin

Product NDC
60760-818
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gabapentin
Dosage form
CAPSULE
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA206943
Marketing category
ANDA
Substance
GABAPENTIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60760-818-6060 CAPSULE in 1 BOTTLE, PLASTIC (60760-818-60) 2023-04-06NoHistorical
60760-818-9090 CAPSULE in 1 BOTTLE, PLASTIC (60760-818-90) 2023-06-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
GabapentinST. MARY'S MEDICAL PARK PHARMACY2023-06-19HUMAN PRESCRIPTION DRUG LABEL2