NDC 54868-2984 Medroxyprogesterone Acetate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2984 - Medroxyprogesterone Acetate
Product Characteristics
Product Packages
NDC Code 54868-2984-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-2984-2
Package Description: 40 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-2984-3
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-2984?
What are the uses for Medroxyprogesterone Acetate?
Which are Medroxyprogesterone Acetate UNII Codes?
The UNII codes for the active ingredients in this product are:
- MEDROXYPROGESTERONE ACETATE (UNII: C2QI4IOI2G)
- MEDROXYPROGESTERONE (UNII: HSU1C9YRES) (Active Moiety)
Which are Medroxyprogesterone Acetate 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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- STARCH, CORN (UNII: O8232NY3SJ)
- LACTOSE (UNII: J2B2A4N98G)
- MINERAL OIL (UNII: T5L8T28FGP)
- SORBIC ACID (UNII: X045WJ989B)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Medroxyprogesterone Acetate?
- RxCUI: 1000114 - medroxyPROGESTERone acetate 10 MG Oral Tablet
- RxCUI: 1000114 - medroxyprogesterone acetate 10 MG Oral Tablet
- RxCUI: 1000135 - medroxyPROGESTERone acetate 2.5 MG Oral Tablet
- RxCUI: 1000135 - medroxyprogesterone acetate 2.5 MG Oral Tablet
- RxCUI: 1000141 - medroxyPROGESTERone acetate 5 MG Oral Tablet
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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".