Gabapentin

Product NDC

50268-349

11-digit product format

502680349

Labeler code

50268

Product ID

50268-349_64b883d0-ef40-651d-e053-2a91aa0a3f40

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

GABAPENTIN

Dosage form

CAPSULE

Route

ORAL

Labeler

AvPAK

Application

ANDA090007

Marketing category

ANDA

Marketing start

2016-03-11

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record