Gabapentin

Product NDC

68071-3244

11-digit product format

680713244

Labeler code

68071

Product ID

68071-3244_4ecb3fe9-c831-5ef0-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gabapentin

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA077661

Marketing category

ANDA

Marketing start

2006-09-15

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

2019-12-31

Current FDA listing

Historical FDA.report record