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Lydia Copper T CU 380A Intrauterine Contraceptive

NAFDAC Reg. No. 03-2634 · Drug

Registered with NAFDAC — registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Lydia Copper T CU 380A Intrauterine Contraceptive
NAFDAC number
03-2634
Active ingredient
Copper intrauterine devices
Strength
NA
Form
NA
Pack size
1 pcs/pack
Manufacturer
Not listed
Applicant (holder)
Deep K. Tyagi Foundation Nigeria
Approved
30 Jan 2025
Status
Active View on NAFDAC ↗
Registration valid to
4 Feb 2030
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • Lydia Copper T CU 380A Intrauterine Contraceptive is on the NAFDAC register with an active registration (03-2634). 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. Not medical advice — always follow your doctor or pharmacist.

What Lydia Copper T CU 380A Intrauterine Contraceptive is used for

From the official U.S. FDA label for copper intrauterine devices, the active ingredient registered with NAFDAC.

What it is used for

For temporary relief of spasms, cramps. Calming effect. May also be use for standard homeopathic indications or as directed by your physician.

Purpose

For temporary relief of spasms, cramps. Calming effect. May also be use for standard homeopathic indications or as directed by your physician.

Do not use if

TAMPER EVIDENT: Do not use if safety seal is broken before first use.

Warnings

Consult your health care provider if symptoms persist more than 5 days or worsen.

Pregnancy & breastfeeding

If pregnant or breastfeeding ask a health professional before use.

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

Check your pack of Lydia Copper T CU 380A Intrauterine Contraceptive

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About Lydia Copper T CU 380A Intrauterine Contraceptive

What is in Lydia Copper T CU 380A Intrauterine Contraceptive?

Lydia Copper T CU 380A Intrauterine Contraceptive contains Copper intrauterine devices (NA), as na, according to its NAFDAC registration record.

Is Lydia Copper T CU 380A Intrauterine Contraceptive registered with NAFDAC?

Yes. Lydia Copper T CU 380A Intrauterine Contraceptive is listed on the NAFDAC register under registration number 03-2634, and its registration is active as of 5 November 2026.

Has Lydia Copper T CU 380A Intrauterine Contraceptive been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Lydia Copper T CU 380A Intrauterine Contraceptive in our automatically synced alert list.

How can I check that my pack of Lydia Copper T CU 380A Intrauterine Contraceptive is genuine?

Run a free authenticity scan with the NAFDAC number 03-2634, 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 Lydia Copper T CU 380A Intrauterine Contraceptive used for?

For temporary relief of spasms, cramps. Calming effect. May also be use for standard homeopathic indications or as directed by your physician. (Summarised from the official U.S. FDA label for copper intrauterine devices. Always follow your doctor or pharmacist.)

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