NDC 67296-0396 Medroxyprogesterone Acetate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 67296-0396?
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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLCELLULOSE (15 MPA.S) (UNII: NPU9M2E6L8)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
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
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Patient Education
Medroxyprogesterone
Medroxyprogesterone is used to treat abnormal menstruation (periods) or irregular vaginal bleeding. Medroxyprogesterone is also used to bring on a normal menstrual cycle in women who menstruated normally in the past but have not menstruated for at least 6 months and who are not pregnant or undergoing menopause (change of life). Medroxyprogesterone is also used to prevent overgrowth of the lining of the uterus (womb) and may decrease the risk of cancer of the uterus in patients who are taking estrogen. Medroxyprogesterone is in a class of medications called progestins. It works by stopping the growth of the lining of the uterus and by causing the uterus to produce certain hormones.
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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".