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Ietrocare Injection

NAFDAC Reg. No. A4-100980 · Drug

Registered with NAFDAC. Registration activeAs of 27 October 2026 · synced automatically from official sources.
Product
Ietrocare Injection
NAFDAC number
A4-100980
Active ingredient
Cetrorelix (Cetrorelix Acetate)
Strength
0.25 mg/0.5 mL
Form
Solution for injection
Pack size
0.5 mL x 1's (in clear PFS with needle)
Manufacturer
Not listed
Applicant (holder)
Ignite Pharma Nigeria Limited
Approved
28 Aug 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Aug 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Ietrocare Injection is on the NAFDAC register with an active registration (A4-100980). 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.

What Ietrocare Injection is used for

From the official U.S. FDA label for cetrorelix (cetrorelix acetate), the active ingredient registered with NAFDAC.

What it is used for

Cetrorelix acetate for injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation.

Possible side effects

The safety of cetrorelix acetate for injection in 949 patients undergoing controlled ovarian stimulation in clinical studies was evaluated. Women were between 19 and 40 years of age (mean: 32). 94.0% of them were Caucasian. Cetrorelix acetate for injection was given in doses ranging from 0.1 mg to 5 mg as either a single or multiple dose. Table 3 shows systemic adverse events, reported in clinical studies without regard to causality, from the beginning of cetrorelix acetate for injection treatment until confirmation of pregnancy by ultrasound at an incidence ≥ 1% in cetrorelix acetate for injection treated subjects undergoing COS. …

Do not use if

Cetrorelix acetate for injection is contraindicated under the following conditions: 1. Hypersensitivity to cetrorelix acetate, extrinsic peptide hormones or mannitol. 2. Known hypersensitivity to GnRH or any other GnRH analogs. 3. Known or suspected pregnancy, and lactation (see PRECAUTIONS). 4. Severe renal impairment.

Warnings

Cetrorelix acetate for injection should be prescribed by physicians who are experienced in fertility treatment. Before starting treatment with cetrorelix acetate for injection, pregnancy must be excluded (see CONTRAINDICATIONS and PRECAUTIONS).

General information only, not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of Ietrocare Injection

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

3 free checks left today Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Ietrocare Injection

What is in Ietrocare Injection?

Ietrocare Injection contains Cetrorelix (Cetrorelix Acetate) (0.25 mg/0.5 mL), as solution for injection, according to its NAFDAC registration record.

Is Ietrocare Injection registered with NAFDAC?

Yes. Ietrocare Injection is listed on the NAFDAC register under registration number A4-100980, and its registration is active as of 27 October 2026.

Has Ietrocare Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Ietrocare Injection in our automatically synced alert list.

How can I check that my pack of Ietrocare Injection is genuine?

Run a free authenticity scan with the NAFDAC number A4-100980, 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.

What is Ietrocare Injection used for?

Cetrorelix acetate for injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation. (Summarised from the official U.S. FDA label for cetrorelix (cetrorelix acetate). Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.