NDC 67046-604 Plavix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67046 - Contract Pharmacy Services-pa
- 67046-604 - Plavix
Product Characteristics
Product Packages
NDC Code 67046-604-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 67046-604?
What are the uses for Plavix?
Which are Plavix UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOPIDOGREL BISULFATE (UNII: 08I79HTP27)
- CLOPIDOGREL (UNII: A74586SNO7) (Active Moiety)
Which are Plavix 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
What is the NDC to RxNorm Crosswalk for Plavix?
- RxCUI: 213169 - Plavix 75 MG Oral Tablet
- RxCUI: 213169 - clopidogrel 75 MG Oral Tablet [Plavix]
- RxCUI: 213169 - Plavix 75 MG (clopidogrel bisulfate 97.875 MG) Oral Tablet
- RxCUI: 309362 - clopidogrel 75 MG Oral Tablet
- RxCUI: 309362 - clopidogrel 75 MG (as clopidogrel bisulfate 97.875 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".