NDC 55379-405 Hybrisil
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What is NDC 55379-405?
What are the uses for Hybrisil?
Which are Hybrisil UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLPREDNISOLONE ACETATE (UNII: 43502P7F0P)
- METHYLPREDNISOLONE (UNII: X4W7ZR7023) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Hybrisil?
- RxCUI: 1100387 - methylPREDNISolone acetate 1 % Topical Gel
- RxCUI: 1100387 - methylprednisolone acetate 0.01 MG/MG Topical Gel
- RxCUI: 1100387 - methylprednisolone acetate 1 % Topical Gel
- RxCUI: 1100391 - HybriSil 1 % Topical Gel
- RxCUI: 1100391 - methylprednisolone acetate 0.01 MG/MG Topical Gel [HybriSil]
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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".