Gabapentin

Product NDC

42292-024

11-digit product format

422920024

Labeler code

42292

Product ID

42292-024_7cd92d1e-9eb1-78da-e053-2991aa0a17f1

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

2016-08-23

Marketing end

0000-00-00

Substance

GABAPENTIN

Active strength

600 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record