NDC 54868-6153 Amitiza
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6153 - Amitiza
Product Characteristics
PINK (C48328)
Product Packages
NDC Code 54868-6153-0
Package Description: 60 CAPSULE, GELATIN COATED in 1 BOTTLE
Product Details
What is NDC 54868-6153?
What are the uses for Amitiza?
Which are Amitiza UNII Codes?
The UNII codes for the active ingredients in this product are:
- LUBIPROSTONE (UNII: 7662KG2R6K)
- LUBIPROSTONE (UNII: 7662KG2R6K) (Active Moiety)
Which are Amitiza 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:
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GELATIN (UNII: 2G86QN327L)
- SORBITOL (UNII: 506T60A25R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- WATER (UNII: 059QF0KO0R)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Amitiza?
- RxCUI: 616578 - lubiprostone 24 MCG Oral Capsule
- RxCUI: 616578 - lubiprostone 0.024 MG Oral Capsule
- RxCUI: 617768 - Amitiza 24 MCG Oral Capsule
- RxCUI: 617768 - lubiprostone 0.024 MG Oral Capsule [Amitiza]
- RxCUI: 617768 - Amitiza 0.024 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".