NDC 54868-6285 Solodyn
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54868-6285?
What are the uses for Solodyn?
Which are Solodyn UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U)
- MINOCYCLINE (UNII: FYY3R43WGO) (Active Moiety)
Which are Solodyn 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:
- HYPROMELLOSE 2910 (50 MPA.S) (UNII: 1IVH67816N)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Solodyn?
- RxCUI: 1013665 - minocycline HCl 80 MG 24HR Extended Release Oral Tablet
- RxCUI: 1013665 - 24 HR minocycline 80 MG Extended Release Oral Tablet
- RxCUI: 1013665 - minocycline 80 MG 24 HR Extended Release Oral Tablet
- RxCUI: 1014024 - SOLODYN 80 MG 24HR Extended Release Oral Tablet
- RxCUI: 1014024 - 24 HR minocycline 80 MG Extended Release Oral Tablet [Solodyn]
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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".