NDC 68071-5052 Amoxicillin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68071 - Nucare Pharmaceuticals,inc.
- 68071-5052 - Amoxicillin
Product Characteristics
Product Packages
NDC Code 68071-5052-3
Package Description: 30 CAPSULE in 1 BOTTLE
Product Details
What is NDC 68071-5052?
What are the uses for Amoxicillin?
Which are Amoxicillin UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMOXICILLIN (UNII: 804826J2HU)
- AMOXICILLIN ANHYDROUS (UNII: 9EM05410Q9) (Active Moiety)
Which are Amoxicillin 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)
- TALC (UNII: 7SEV7J4R1U)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
What is the NDC to RxNorm Crosswalk for Amoxicillin?
- RxCUI: 308191 - amoxicillin 500 MG Oral Capsule
- RxCUI: 308191 - amoxicillin (as amoxicillin trihydrate) 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".