Gabapentin

Product NDC

70518-0781

11-digit product format

705180781

Labeler code

70518

Product ID

70518-0781_8ec850d9-c4c7-95b9-e053-2995a90acb57

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Gabapentin

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA202764

Marketing category

ANDA

Marketing start

2017-10-11

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