NDC 71205-902 Progesterone
Capsule Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71205 - Proficient Rx Lp
- 71205-902 - Progesterone
Product Characteristics
Product Packages
NDC Code 71205-902-11
Package Description: 1000 CAPSULE in 1 BOTTLE
NDC Code 71205-902-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 71205-902-55
Package Description: 500 CAPSULE in 1 BOTTLE
NDC Code 71205-902-60
Package Description: 60 CAPSULE in 1 BOTTLE
NDC Code 71205-902-72
Package Description: 120 CAPSULE in 1 BOTTLE
NDC Code 71205-902-90
Package Description: 90 CAPSULE in 1 BOTTLE
Product Details
What is NDC 71205-902?
What are the uses for Progesterone?
What are Progesterone Active Ingredients?
- PROGESTERONE 100 mg/1 - The major progestational steroid that is secreted primarily by the CORPUS LUTEUM and the PLACENTA. Progesterone acts on the UTERUS, the MAMMARY GLANDS and the BRAIN. It is required in EMBRYO IMPLANTATION; PREGNANCY maintenance, and the development of mammary tissue for MILK production. Progesterone, converted from PREGNENOLONE, also serves as an intermediate in the biosynthesis of GONADAL STEROID HORMONES and adrenal CORTICOSTEROIDS.
Which are Progesterone UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROGESTERONE (UNII: 4G7DS2Q64Y)
- PROGESTERONE (UNII: 4G7DS2Q64Y) (Active Moiety)
Which are Progesterone 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:
- PEANUT OIL (UNII: 5TL50QU0W4)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
What is the NDC to RxNorm Crosswalk for Progesterone?
- RxCUI: 260243 - progesterone 100 MG Oral Capsule
- RxCUI: 312641 - progesterone 200 MG Oral Capsule
Which are the Pharmacologic Classes for Progesterone?
* Please review the disclaimer below.
Patient Education
Progesterone
Progesterone is used as a part of hormone replacement therapy in women who have passed menopause (the change of life) and have not had a hysterectomy (surgery to remove the uterus). Hormone replacement therapy usually includes estrogen, which is used to treat symptoms of menopause and reduce the risk of developing certain diseases. However, estrogen can also cause abnormal thickening of the lining of the uterus and increase the risk of developing uterine cancer. Progesterone helps to prevent this thickening and decreases the risk of developing uterine cancer. Progesterone is also used to bring on menstruation (period) in women of childbearing age who have had normal periods and then stopped menstruating. Progesterone is in a class of medications called progestins (female hormones). It works as part of hormone replacement therapy by decreasing the amount of estrogen in the uterus. It works to bring on menstruation by replacing the natural progesterone that some women are missing.
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Progestin-Only (norethindrone) Oral Contraceptives
Progestin-only (norethindrone) oral contraceptives are used to prevent pregnancy. Progestin is a female hormone. It works by preventing the release of eggs from the ovaries (ovulation) and changing the cervical mucus and the lining of the uterus. Progestin-only (norethindrone) oral contraceptives are a very effective method of birth control, but they do not prevent the spread of AIDS and other sexually transmitted diseases.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".