NDC 67296-0122 Dicloxacillin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329)
Code Structure Chart
Product Details
What is NDC 67296-0122?
What are the uses for Dicloxacillin Sodium?
Which are Dicloxacillin Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- DICLOXACILLIN SODIUM (UNII: 4HZT2V9KX0)
- DICLOXACILLIN (UNII: COF19H7WBK) (Active Moiety)
Which are Dicloxacillin Sodium 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Dicloxacillin Sodium?
- RxCUI: 197596 - dicloxacillin sodium 500 MG Oral Capsule
- RxCUI: 197596 - dicloxacillin 500 MG Oral Capsule
- RxCUI: 197596 - dicloxacillin (as dicloxacillin sodium) 500 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".