NDC 54868-5234 Griseofulvin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5234 - Griseofulvin
Product Packages
NDC Code 54868-5234-0
Package Description: 120 mL in 1 BOTTLE
Product Details
What is NDC 54868-5234?
What are the uses for Griseofulvin?
Which are Griseofulvin UNII Codes?
The UNII codes for the active ingredients in this product are:
- GRISEOFULVIN (UNII: 32HRV3E3D5)
- GRISEOFULVIN (UNII: 32HRV3E3D5) (Active Moiety)
Which are Griseofulvin 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:
- ALCOHOL (UNII: 3K9958V90M)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- MENTHOL (UNII: L7T10EIP3A)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- SUCROSE (UNII: C151H8M554)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Griseofulvin?
- RxCUI: 239238 - griseofulvin 125 MG in 5 mL Oral Suspension
- RxCUI: 239238 - griseofulvin 25 MG/ML Oral Suspension
- RxCUI: 239238 - griseofulvin 125 MG per 5 ML Oral Suspension
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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".