NDC 67296-0570 Prochlorperazine Maleate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67296 - Redpharm Drug, Inc.
- 67296-0570 - Prochlorperazine Maleate
Product Characteristics
Product Packages
NDC Code 67296-0570-2
Package Description: 15 TABLET in 1 BOTTLE
NDC Code 67296-0570-3
Package Description: 10 TABLET in 1 BOTTLE
Product Details
What is NDC 67296-0570?
What are the uses for Prochlorperazine Maleate?
Which are Prochlorperazine Maleate UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROCHLORPERAZINE MALEATE (UNII: I1T8O1JTL6)
- PROCHLORPERAZINE (UNII: YHP6YLT61T) (Active Moiety)
Which are Prochlorperazine Maleate 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:
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- STARCH, CORN (UNII: O8232NY3SJ)
- TRIACETIN (UNII: XHX3C3X673)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Prochlorperazine Maleate?
- RxCUI: 198365 - prochlorperazine maleate 10 MG Oral Tablet
- RxCUI: 198365 - prochlorperazine 10 MG Oral Tablet
- RxCUI: 198365 - prochlorperazine (as prochlorperazine maleate) 10 MG Oral Tablet
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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".