FDA Label for Chlorpromazine Hydrochloride
View Indications, Usage & Precautions
Chlorpromazine Hydrochloride Product Label
The following document was submitted to the FDA by the labeler of this product Zydus Lifesciences Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Package Label.Principal Display Panel
NDC 70771-1778-1
chlorproMAZINE Hydrochloride Injection, USP
25 mg/mL
For Deep Intramuscular Use
Discard unused portion
1 mL Single-Dose Vial
Rx only
NDC 70771-1778-7
chlorproMAZINE Hydrochloride Injection, USP
25 mg/mL
For Deep Intramuscular Use
Discard unused portion
25 x 1 mL Single-Dose Vial
Rx only
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