NDC 54868-5934 Menest
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ORANGE (C48331)
M73
Code Structure Chart
Product Details
What is NDC 54868-5934?
What are the uses for Menest?
Which are Menest UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESTROGENS, ESTERIFIED (UNII: 3ASP8Q3768)
- ESTROGENS, ESTERIFIED (UNII: 3ASP8Q3768) (Active Moiety)
Which are Menest 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:
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SHELLAC (UNII: 46N107B71O)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- VANILLIN (UNII: CHI530446X)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Menest?
- RxCUI: 197666 - estrogens, esterified 0.3 MG Oral Tablet
- RxCUI: 197666 - estrogens, esterified (USP) 0.3 MG Oral Tablet
- RxCUI: 197667 - estrogens, esterified 0.625 MG Oral Tablet
- RxCUI: 197667 - estrogens, esterified (USP) 0.625 MG Oral Tablet
- RxCUI: 197668 - estrogens, esterified 1.25 MG Oral Tablet
* 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".