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NDC 70710-1131-01

Chlorpromazine hydrochloride 50 mg/1 TABLET, FILM COATED

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NDC
70710-1131-01
Generic Name
Chlorpromazine hydrochloride
Brand Name
Chlorpromazine hydrochloride
Strength
50 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Package Size
—
Labeler
Zydus Pharmaceuticals (USA) Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE For the management of manifestations of psychotic disorders. For the treatment of schizophrenia. To control nausea and vomiting. For relief of restlessness and apprehension before surgery. For acute intermittent porphyria. As an adjunct in the treatment of tetanus. To control the manifestations of the manic type of manic-depressive illness. For relief of intractable hiccups. For the treatment of severe behavioral problems in children (1 to 12 years of age) marked by combati…

Important Warnings

WARNINGS Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Chlorpromazine hydrochloride is not approved for the treatment of patients with dementia-related psychosis (see BOXED WARNING). The extrapyramidal symptoms which can occur secondary to chlorpromazine ma…

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

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Other Chlorpromazine hydrochloride NDC Codes

70710-1133-01200 mg/1TABLET, FILM COATED
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72205-0107-91200 mg/1TABLET, SUGAR COATED
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55150-0319-2525 mg/mLINJECTION
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68462-0863-0150 mg/1TABLET, FILM COATED
2-Day

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