NDC 63629-8444 Compro
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63629 - Bryant Ranch Prepack
- 63629-8444 - Compro
Product Characteristics
Product Packages
NDC Code 63629-8444-1
Package Description: 12 PACKET in 1 CARTON / 1 SUPPOSITORY in 1 PACKET
Product Details
What is NDC 63629-8444?
What are the uses for Compro?
Which are Compro UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROCHLORPERAZINE (UNII: YHP6YLT61T)
- PROCHLORPERAZINE (UNII: YHP6YLT61T) (Active Moiety)
Which are Compro 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL PALMITATE (UNII: 6Y2XJ05B35)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)
What is the NDC to RxNorm Crosswalk for Compro?
- RxCUI: 198159 - prochlorperazine 25 MG Rectal Suppository
- RxCUI: 284254 - Compro 25 MG Rectal Suppository
- RxCUI: 284254 - prochlorperazine 25 MG Rectal Suppository [Compro]
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Patient Education
Prochlorperazine
Prochlorperazine suppositories and tablets are used to control severe nausea and vomiting. Prochlorperazine tablets are also 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). Prochlorperazine tablets are also used on a short-term basis to treat anxiety that could not be controlled by other medications. Prochlorperazine should not be used to treat any condition in children who are younger than 2 years old or who weigh less than 20 pounds (about 9 kilograms). Prochlorperazine is in a class of medications called conventional antipsychotics. It works by decreasing abnormal excitement in the brain.
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[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".