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Home / Registered in Nigeria / Chorionic Gonadotropin for Injection USP 5000 IU

Chorionic Gonadotropin for Injection USP 5000 IU

NAFDAC Reg. No. A6-100121 · Drug

Registered with NAFDAC. Registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
Chorionic Gonadotropin for Injection USP 5000 IU
NAFDAC number
A6-100121
Active ingredient
Chorionic gonadotrophin
Strength
5000 IU
Form
Powder for injection
Pack size
5000 IU x 1's (in clear glass vial) + 0.9% w/v Sodium Chloride Injection USP as diluent (in ampoule)
Manufacturer
Not listed
Applicant (holder)
Ignite Pharma Nigeria Limited
Approved
3 Jul 2023
Status
Active View on NAFDAC ↗
Registration valid to
2 Jul 2028
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Chorionic gonadotrophin: uses, dosage and brands worldwide

What we found

  • Chorionic Gonadotropin for Injection USP 5000 IU is on the NAFDAC register with an active registration (A6-100121). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Chorionic Gonadotropin for Injection USP 5000 IU

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

HCG HAS NOT BEEN DEMONSTRATED TO BE EFFECTIVE ADJUNCTIVE THERAPY IN THE TREATMENT OF OBESITY. THERE IS NO SUBSTANTIAL EVIDENCE THAT IT INCREASES WEIGHT LOSS BEYOND THAT RESULTING FROM CALORIC RESTRICTION, THAT IT CAUSES A MORE ATTRACTIVE OR ‘‘NORMAL’’ DISTRIBUTION OF FAT, OR THAT IT DECREASES THE HUNGER AND DISCOMFORT ASSOCIATED WITH CALORIE-RESTRICTED DIETS. Prepubertal cryptorchidism not due to anatomical obstruction. In general, HCG is thought to induce testicular descent in situations when descent would have occurred at puberty. HCG thus may help predict whether or not orchiopexy will be needed in the future. …

How to take it and how often
  • Intramuscular Use Only The dosage regimen employed in any particular case will depend upon the indication for use, the age and weight of the patient and the physician’s preference
  • The following regimens have been advocated by various authorities
  • Prepubertal Cryptorchidism Not Due To Anatomical Obstruction 4,000 USP units three times weekly for three weeks. 5,000 USP units every second day for four injections. 15 injections of 500 to 1,000 USP units over a period of six weeks. 500 USP units three times weekly for four to six weeks
  • If this course of treatment is not successful, another is begun one month later giving 1,000 USP units per injection
  • Selected Cases Of Hypogonadotropic Hypogonadism In Males 500 to 1,000 USP units three times a week for three weeks, followed by the same dose twice a week for three weeks. 4,000 USP units three times weekly for six to nine months, following which the dosage may be reduced to 2,000 USP units three times weekly for an additional three months
  • Induction of ovulation and pregnancy in the anovulatory, infertile woman in whom the cause of anovulation is secondary and not due to primary ovarian failure and who has been appropriately pretreated with human menotropins (see prescribing information for menotropins for dosage and administration for that drug product). 5,000 to 10,000 USP units one day following the last dose of menotropins. (A dosage of 10,000 units is recommended in the labeling for menotropins.) IMPORTANT: USE COMPLETELY WITHIN 60 DAYS AFTER RECONSTITUTION
  • REFRIGERATE AFTER RECONSTITUTION. …
Talk to a doctor first if

Precocious puberty, prostatic carcinoma or other androgen-dependent neoplasm, prior allergic reaction to HCG.

Warnings

HCG should be used in conjunction with human menopausal gonadotropins only by physicians experienced with infertility problems who are familiar with the criteria for patient selection, contraindications, warnings, precautions and adverse reactions described in the package insert for menotropins. The principal serious adverse reactions are: (1) Ovarian hyperstimulation, a syndrome of sudden ovarian enlargement, ascites with or without pain and/or pleural effusion, (2) Rupture of ovarian cysts with resultant hemoperitoneum, (3) Multiple births and (4) Arterial thromboembolism. Anaphylaxis and other hypersensitivity reactions have been reported with urinary-derived HCG products.

Possible side effects

Headache, irritability, restlessness, depression, fatigue, edema, precocious puberty, gynecomastia and pain at the site of injection.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2025-03-25.

Label for chorionic gonadotrophin, the active ingredient registered with NAFDAC.

Check your pack of Chorionic Gonadotropin for Injection USP 5000 IU

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Chorionic Gonadotropin for Injection USP 5000 IU

What is in Chorionic Gonadotropin for Injection USP 5000 IU?

Chorionic Gonadotropin for Injection USP 5000 IU contains Chorionic gonadotrophin (5000 IU), as powder for injection, according to its NAFDAC registration record.

Is Chorionic Gonadotropin for Injection USP 5000 IU registered with NAFDAC?

Yes. Chorionic Gonadotropin for Injection USP 5000 IU is listed on the NAFDAC register under registration number A6-100121, and its registration is active as of 6 November 2026.

Has Chorionic Gonadotropin for Injection USP 5000 IU been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Chorionic Gonadotropin for Injection USP 5000 IU in our automatically synced alert list.

How can I check that my pack of Chorionic Gonadotropin for Injection USP 5000 IU is genuine?

Run a free authenticity scan with the NAFDAC number A6-100121, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Chorionic Gonadotropin for Injection USP 5000 IU?

Follow your prescription or the leaflet in your pack. The official label says: Intramuscular Use Only The dosage regimen employed in any particular case will depend upon the indication for use, the age and weight of the patient and the physician’s preference. The following regimens have been advocated by various authorities. Prepubertal Cryptorchidism Not Due To Anatomical Obstruction 4,000 USP units three times weekly for three weeks. 5,000 USP units eve…

What is Chorionic Gonadotropin for Injection USP 5000 IU used for?

HCG HAS NOT BEEN DEMONSTRATED TO BE EFFECTIVE ADJUNCTIVE THERAPY IN THE TREATMENT OF OBESITY. THERE IS NO SUBSTANTIAL EVIDENCE THAT IT INCREASES WEIGHT LOSS BEYOND THAT RESULTING FROM CALORIC RESTRICTION, THAT IT CAUSES A MORE ATTRACTIVE OR ‘‘NORMAL’’ DISTRIBUTION OF FAT, OR THAT IT DECREASES THE HUNGER AND DISCOMFORT ASSOCIATED WITH CALORIE-RESTRICTED DIETS. Prepubertal cryptorchidism not due to (Summarised from the official U.S. FDA label for chorionic gonadotrophin. Always follow your doctor or pharmacist.)

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