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NDC 70010-0770-05

Methocarbamol Tablets 750 mg/1 TABLET, COATED

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NDC
70010-0770-05
Generic Name
Methocarbamol Tablets
Brand Name
Methocarbamol
Strength
750 mg/1
Dosage Form
TABLET, COATED
Route
ORAL
Package Size
—
Labeler
Granules Pharmaceuticals Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Methocarbamol tablets, USP 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 should be cautioned about combined effects with alcohol and other CNS depressants. Safe use of Methocarbamol tablets has not been established with regard to possible adverse effects upon fetal development. There have been reports of fetal and congenital abnormalities following in uter…

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

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Other Methocarbamol Tablets NDC Codes

70010-0754-05500 mg/1TABLET, COATED
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70010-0754-01500 mg/1TABLET, COATED
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70010-0770-01750 mg/1TABLET, COATED
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