NDC 68645-430 Clopidogrel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68645 - Legacy Pharmaceutical Packaging
- 68645-430 - Clopidogrel
Product Characteristics
Product Packages
NDC Code 68645-430-54
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 68645-430?
What are the uses for Clopidogrel?
Which are Clopidogrel UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOPIDOGREL BISULFATE (UNII: 08I79HTP27)
- CLOPIDOGREL (UNII: A74586SNO7) (Active Moiety)
Which are Clopidogrel 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:
- CROSPOVIDONE (UNII: 68401960MK)
- HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- COCHINEAL (UNII: TZ8Z31B35M)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- LACTOSE (UNII: J2B2A4N98G)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Clopidogrel?
- RxCUI: 309362 - clopidogrel 75 MG Oral Tablet
- RxCUI: 309362 - clopidogrel 75 MG (as clopidogrel bisulfate 97.875 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".