NDC 67296-1291 Cefdinir
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLUE (C48333 - TEAL OPAQUE)
Code Structure Chart
Product Details
What is NDC 67296-1291?
What are the uses for Cefdinir?
Which are Cefdinir UNII Codes?
The UNII codes for the active ingredients in this product are:
- CEFDINIR MONOHYDRATE (UNII: 6E7SN358SE)
- CEFDINIR (UNII: CI0FAO63WC) (Active Moiety)
Which are Cefdinir 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:
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- CARBOXYMETHYLCELLULOSE CALCIUM (UNII: UTY7PDF93L)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- SHELLAC (UNII: 46N107B71O)
- ALCOHOL (UNII: 3K9958V90M)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AMMONIA (UNII: 5138Q19F1X)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
What is the NDC to RxNorm Crosswalk for Cefdinir?
- RxCUI: 200346 - cefdinir 300 MG Oral Capsule
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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".