GABAPENTIN

Product NDC

61919-411

11-digit product format

619190411

Labeler code

61919

Product ID

61919-411_9c9436ae-7dbd-1c16-e053-2a95a90a3238

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

GABAPENTIN

Dosage form

CAPSULE

Route

ORAL

Labeler

DIRECT RX

Application

ANDA090705

Marketing category

ANDA

Marketing start

2018-03-15

Marketing end

0000-00-00

Substance

GABAPENTIN

Active strength

300 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record