Methocarbamol

Product NDC

53808-0956

11-digit product format

538080956

Labeler code

53808

Product ID

53808-0956_27a1eeb9-0064-48f8-9e34-91fdb455e818

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

methocarbamol

Dosage form

TABLET

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA040489

Marketing category

ANDA

Marketing start

2014-01-01

Marketing end

0000-00-00

Substance

METHOCARBAMOL

Active strength

750 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