NDC 12634-418 Promethazine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 12634-418-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 12634-418-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 12634-418-40
Package Description: 40 TABLET in 1 BOTTLE
NDC Code 12634-418-52
Package Description: 12 TABLET in 1 BLISTER PACK
NDC Code 12634-418-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 12634-418-61
Package Description: 10 TABLET in 1 BLISTER PACK
NDC Code 12634-418-65
Package Description: 5 TABLET in 1 BLISTER PACK
NDC Code 12634-418-66
Package Description: 6 TABLET in 1 BLISTER PACK
NDC Code 12634-418-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-418-74
Package Description: 24 TABLET in 1 BOTTLE
NDC Code 12634-418-80
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 12634-418-82
Package Description: 12 TABLET in 1 BOTTLE
NDC Code 12634-418-85
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 12634-418-91
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 12634-418-92
Package Description: 2 TABLET in 1 BOTTLE
NDC Code 12634-418-94
Package Description: 4 TABLET in 1 BOTTLE
NDC Code 12634-418-95
Package Description: 5 TABLET in 1 BOTTLE
NDC Code 12634-418-96
Package Description: 6 TABLET in 1 BOTTLE
NDC Code 12634-418-99
Package Description: 9 TABLET in 1 BOTTLE
Product Details
What is NDC 12634-418?
What are the uses for Promethazine Hydrochloride?
Which are Promethazine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROMETHAZINE HYDROCHLORIDE (UNII: R61ZEH7I1I)
- PROMETHAZINE (UNII: FF28EJQ494) (Active Moiety)
Which are Promethazine 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Promethazine Hydrochloride?
- RxCUI: 992447 - promethazine HCl 25 MG Oral Tablet
- RxCUI: 992447 - promethazine hydrochloride 25 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Promethazine
Promethazine is used to relieve the symptoms of allergic reactions such as allergic rhinitis (runny nose and watery eyes caused by allergy to pollen, mold or dust), allergic conjunctivitis (red, watery eyes caused by allergies), allergic skin reactions, and allergic reactions to blood or plasma products. Promethazine is used with other medications to treat anaphylaxis (sudden, severe allergic reactions) and the symptoms of the common cold such as sneezing, cough, and runny nose. Promethazine is also used to relax and sedate patients before and after surgery, during labor, and at other times. Promethazine is also used to prevent and control nausea and vomiting that may occur after surgery, and with other medications to help relieve pain after surgery. Promethazine is also used to prevent and treat motion sickness. Promethazine helps control symptoms, but will not treat the cause of the symptoms or speed recovery. Promethazine is in a class of medications called phenothiazines. It works by blocking the action of a certain natural substance in the body.
[Learn More]
* 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".