Gabapentin

Product NDC

0143-9994

11-digit product format

001439994

Labeler code

0143

Product ID

0143-9994_02f23e78-3140-458b-9955-021229fb1d67

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gabapentin

Dosage form

CAPSULE

Route

ORAL

Labeler

West-ward Pharmaceutical Corp

Application

ANDA078150

Marketing category

ANDA

Marketing start

2007-07-09

Marketing end

0000-00-00

Substance

GABAPENTIN

Active strength

400 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record