Gabapentin

Product NDC

63739-675

11-digit product format

637390675

Labeler code

63739

Product ID

63739-675_690c2e25-cb21-47d8-8f76-9fe6f1c1932c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gabapentin

Dosage form

CAPSULE

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA078428

Marketing category

ANDA

Marketing start

2009-11-24

Marketing end

0000-00-00

Substance

GABAPENTIN

Active strength

100 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