NDC 54868-1729 Depo-estradiol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-1729 - Depo-estradiol
Product Packages
NDC Code 54868-1729-0
Package Description: 1 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Details
What is NDC 54868-1729?
What are the uses for Depo-estradiol?
Which are Depo-estradiol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ESTRADIOL CYPIONATE (UNII: 7E1DV054LO)
- ESTRADIOL CYPIONATE (UNII: 7E1DV054LO) (Active Moiety)
Which are Depo-estradiol 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:
- COTTONSEED OIL (UNII: H3E878020N)
What is the NDC to RxNorm Crosswalk for Depo-estradiol?
- RxCUI: 206417 - Depo-Estradiol 5 MG/ML Injectable Solution
- RxCUI: 206417 - estradiol cypionate 5 MG/ML Injectable Solution [Depo-estradiol]
- RxCUI: 310187 - estradiol cypionate 5 MG/ML Injectable Solution
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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".