NDC 70882-123 Clopidogrel Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330)
6 MM
L
Code Structure Chart
Product Details
What is NDC 70882-123?
What are the uses for Clopidogrel Kit?
Which are Clopidogrel Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLOPIDOGREL BISULFATE (UNII: 08I79HTP27)
- CLOPIDOGREL (UNII: A74586SNO7) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Clopidogrel Kit 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
- METHYLCELLULOSE (15 MPA.S) (UNII: NPU9M2E6L8)
- ZINC STEARATE (UNII: H92E6QA4FV)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYDROXYPROPYL CELLULOSE (1200000 MW) (UNII: RFW2ET671P)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- TRIACETIN (UNII: XHX3C3X673)
- METHACRYLIC ACID (UNII: 1CS02G8656)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
What is the NDC to RxNorm Crosswalk for Clopidogrel Kit?
- RxCUI: 308416 - aspirin 81 MG Delayed Release Oral Tablet
- RxCUI: 308416 - ASA 81 MG Delayed Release Oral Tablet
- RxCUI: 308416 - aspirin 81 MG Enteric Coated 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".