Methocarbamol

Product NDC

55700-630

11-digit product format

557000630

Labeler code

55700

Product ID

55700-630_126928d1-aae2-4c01-b9c3-5bd1911891a5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methocarbamol

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA200958

Marketing category

ANDA

Marketing start

2018-05-25

Marketing end

0000-00-00

Substance

METHOCARBAMOL

Active strength

500 mg/1

Pharmacologic classes

Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record