NDC 50090-2865 Chlorpromazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-2865 - Chlorpromazine Hydrochloride
Product Characteristics
Product Packages
NDC Code 50090-2865-0
Package Description: 32 TABLET, SUGAR COATED in 1 BOTTLE, UNIT-DOSE
Product Details
What is NDC 50090-2865?
What are the uses for Chlorpromazine Hydrochloride?
Which are Chlorpromazine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORPROMAZINE HYDROCHLORIDE (UNII: 9WP59609J6)
- CHLORPROMAZINE (UNII: U42B7VYA4P) (Active Moiety)
Which are Chlorpromazine Hydrochloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ACACIA (UNII: 5C5403N26O)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CALCIUM SULFATE, UNSPECIFIED FORM (UNII: WAT0DDB505)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SHELLAC (UNII: 46N107B71O)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Chlorpromazine Hydrochloride?
- RxCUI: 991044 - chlorproMAZINE HCl 100 MG Oral Tablet
- RxCUI: 991044 - chlorpromazine hydrochloride 100 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Chlorpromazine
Chlorpromazine is used to treat the symptoms of schizophrenia (a mental illness that causes disturbed or unusual thinking, loss of interest in life, and strong or inappropriate emotions) and other psychotic disorders (conditions that cause difficulty telling the difference between things or ideas that are real and things or ideas that are not real) and to treat the symptoms of mania (frenzied, abnormally excited mood) in people who have bipolar disorder (manic depressive disorder; a condition that causes episodes of mania, episodes of depression, and other abnormal moods). Chlorpromazine is also used to treat severe behavior problems such as explosive, aggressive behavior and hyperactivity in children 1 to 12 years of age. Chlorpromazine is also used to control nausea and vomiting, to relieve hiccups that have lasted one month or longer, and to relieve restlessness and nervousness that may occur just before surgery. Chlorpromazine is also used to treat acute intermittent porphyria (condition in which certain natural substances build up in the body and cause stomach pain, changes in thinking and behavior, and other symptoms). Chlorpromazine is also used along with other medications to treat tetanus (a serious infection that may cause tightening of the muscles, especially the jaw muscle). Chlorpromazine is in a class of medications called conventional antipsychotics. It works by changing the activity of certain natural substances in the brain and other parts of the body.
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* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".