NDC 11528-020 Covaryx HS
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11528 - Centrix Pharmaceutical, Inc,
- 11528-020 - Covaryx
Product Characteristics
Product Packages
NDC Code 11528-020-01
Package Description: 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11528-020?
What are the uses for Covaryx HS?
Which are Covaryx HS UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESTROGENS, ESTERIFIED (UNII: 3ASP8Q3768)
- ESTROGENS, ESTERIFIED (UNII: 3ASP8Q3768) (Active Moiety)
- METHYLTESTOSTERONE (UNII: V9EFU16ZIF)
- METHYLTESTOSTERONE (UNII: V9EFU16ZIF) (Active Moiety)
Which are Covaryx HS 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:
- TALC (UNII: 7SEV7J4R1U)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FOOD YELLOW 3 FREE ACID (UNII: G2B7JWK1GG)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
What is the NDC to RxNorm Crosswalk for Covaryx HS?
- RxCUI: 197670 - estrogens, esterified 1.25 MG / methylTESTOSTERone 2.5 MG Oral Tablet
- RxCUI: 197670 - estrogens, esterified (USP) 1.25 MG / methyltestosterone 2.5 MG Oral Tablet
- RxCUI: 197670 - EEMT DS Oral Tablet
- RxCUI: 238006 - estrogens, esterified 0.625 MG / methylTESTOSTERone 1.25 MG Oral Tablet
- RxCUI: 238006 - estrogens, esterified (USP) 0.625 MG / methyltestosterone 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".