Gabapentin

Product NDC

42292-025

11-digit product format

422920025

Labeler code

42292

Product ID

42292-025_9aee1f84-b52d-09a6-e053-2a95a90ae4d8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gabapentin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA200651

Marketing category

ANDA

Marketing start

2016-08-22

Marketing end

2020-12-31

Substance

GABAPENTIN

Active strength

800 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record