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NDC 76385-0124-01

Methocarbamol 750 mg/1 TABLET, FILM COATED

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NDC
76385-0124-01
Generic Name
Methocarbamol
Brand Name
Methocarbamol
Strength
750 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
Labeler
UNICHEM PHARMACEUTICALS (USA), INC.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Methocarbamol Tablets USP, 500 mg and 750 mg are indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute, painful musculoskeletal conditions. The mode of action of methocarbamol has not been clearly identified, but may be related to its sedative properties. Methocarbamol does not directly relax tense skeletal muscles in man.

Important Warnings

WARNINGS Since methocarbamol may possess a general CNS depressant effect, patients receiving Methocarbamol Tablets USP, 500 mg or 750 mg should be cautioned about combined effects with alcohol and other CNS depressants. Safe use of Methocarbamol Tablets USP, 500 mg and 750 mg has not been established with regard to possible adverse effects upon fetal development. There have been reports of fetal a…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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