NDC 54868-0654 Clarithromycin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0654 - Clarithromycin
Product Packages
NDC Code 54868-0654-0
Package Description: 100 mL in 1 BOTTLE
NDC Code 54868-0654-1
Package Description: 50 mL in 1 BOTTLE
Product Details
What is NDC 54868-0654?
What are the uses for Clarithromycin?
Which are Clarithromycin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLARITHROMYCIN (UNII: H1250JIK0A)
- CLARITHROMYCIN (UNII: H1250JIK0A) (Active Moiety)
Which are Clarithromycin 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POVIDONE (UNII: FZ989GH94E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Clarithromycin?
- RxCUI: 309322 - clarithromycin 250 MG in 5 mL Oral Suspension
- RxCUI: 309322 - clarithromycin 50 MG/ML Oral Suspension
- RxCUI: 309322 - clarithromycin 250 MG per 5 ML Oral Suspension
* 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".