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Drug Catalog - Product Detail

PROGESTERONE USP IN SESAME OIL FOR INJECTION INJECT. 50MG/10ML 1X10ML

NDC Mfr Size Str Form
00591-3128-79 ACTAVIS PHARMA 10 50MG/ML OIL
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PACKAGE FILES

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Generic Name
PROGESTERONE
Substance Name
PROGESTERONE
Product Type
HUMAN PRESCRIPTION DRUG
Route
INTRAMUSCULAR
Application Number
NDA017362
Description
DESCRIPTION Progesterone injection, a progestin, is a sterile solution of progesterone in a suitable vegetable oil available for intramuscular use. Progesterone occurs as a white or creamy white, crystalline powder. It is odorless and is stable in air. Practically insoluble in water, it is soluble in alcohol, acetone, and dioxane and sparingly soluble in vegetable oils. It has the following structural formula: C 21 H 30 O 2 M.W. 314.47 Pregn-4-ene-3, 20-dione Each mL contains: Progesterone 50 mg, Benzyl Alcohol 10% as preservative in Sesame Oil q.s. Progesterone structural formula.
How Supplied
HOW SUPPLIED Progesterone Injection USP, 500 mg/10 mL (50 mg/mL) is available in 10 mL multiple dose vials, individually boxed. (NDC 0591-3128-79) Store at 20°-25°C (68°-77°F). [See USP controlled room temperature.] Rx only For all medical inquiries contact: ACTAVIS Medical Communications Parsippany, NJ 07054 800-272-5525 Distributed By: Actavis Pharma, Inc. Parsippany, NJ 07054 USA Manufactured By: Hikma Farmacêutica Fervença 2705-906 Terrugem SNT Portugal Revised:August 2018
Indications & Usage
INDICATIONS AND USAGE This drug is indicated in amenorrhea and abnormal uterine bleeding due to hormonal imbalance in the absence of organic pathology, such as submucous fibroids or uterine cancer.
Dosage and Administration
DOSAGE AND ADMINISTRATION Progesterone is administered by intramuscular injection. It differs from other commonly used steroids in that it is irritating at the place of injection. Amenorrhea: Five to 10 mg are given for six to eight consecutive days. If there has been sufficient ovarian activity to produce a proliferative endometrium, one can expect withdrawal bleeding forty-eight to seventy-two hours after the last injection. This may be followed by spontaneous normal cycles. Functional Uterine Bleeding: Five to 10 mg are given daily for six doses. Bleeding may be expected to cease within six days. When estrogen is given as well, the administration of progesterone is begun after two weeks of estrogen therapy. If menstrual flow begins during the course of injections of progesterone, they are discontinued. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever the solution and container permit.