NDC 68151-2480 Chlorpromazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
8 MM
832;10
Code Structure Chart
Product Details
What is NDC 68151-2480?
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: 991039 - chlorproMAZINE HCl 10 MG Oral Tablet
- RxCUI: 991039 - chlorpromazine hydrochloride 10 MG Oral Tablet
- RxCUI: 991336 - chlorproMAZINE HCl 50 MG Oral Tablet
- RxCUI: 991336 - chlorpromazine hydrochloride 50 MG Oral Tablet
* 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".