Progesterone Suppository

Name: Progesterone Suppository
Brand: Artemisine Medicines Technology Co., Ltd.

Suppositories

Progesterone Suppository — GMP manufactured suppositories by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product Name	Progesterone Suppository
Dosage Form	Suppositories
Strength	25 mg
Standards	BP / ENTERPRISE
Packing	Customized per market requirement (bottle / blister / box)
Documents	COA, COPP, DMF, CTD Dossiers
MOQ	Contact us for MOQ and current stock

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WHO Prescribing Guidance

Indications · Administration · Dosage · Precautions

Reference information summarised from WHO prescribing guidance. Expand each item below — clinical use must always follow the locally approved product insert.

🎯Indications▾

Hormone replacement therapy, menstrual disorders, endometriosis, threatened or recurrent miscarriage (according to local guidance) and, for some progestins, contraception.

💧Administration▾

Oral capsules/tablets, IM depot injection or vaginal route depending on the product; take oral doses at the same time each day.

⚖️Dosage▾

Product- and indication-specific: e.g. norethisterone 5 mg 2–3 times daily for menstrual disorders; medroxyprogesterone acetate 10 mg daily in HRT. Follow the approved indication-specific schedule.

⚠️Precautions & Warnings▾

Avoid in pregnancy (except where specifically indicated), breast cancer, hepatic tumours and unexplained vaginal bleeding. May cause fluid retention, headache and mood change; report severe leg pain or visual disturbance.

Reference: WHO Model Formulary / WHO Model List of Essential Medicines. For professional reference only — clinical use must follow the locally approved product insert and national treatment guidelines.

Why Order From Us

Factory Direct. Fully Documented.

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GMP Quality

Full batch testing and quality traceability under standard GMP workshops.

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Fast Delivery

Sufficient stock on regular items, familiar with export logistics to 50+ countries.

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Registration Support

COA, DMF, dossier and legalization documents for your market registration.

FAQ

Progesterone Suppository — Frequently Asked Questions

Which documents are provided for Progesterone Suppository registration?

Every batch of Progesterone Suppository ships with a Certificate of Analysis (COA). For market registration we provide COPP, DMF and CTD-format dossiers, plus legalisation support where your authority requires it.

What is the MOQ and lead time for Progesterone Suppository?

MOQ and lead time for Progesterone Suppository depend on strength, packaging and destination market. Send us your target market and annual volume — our export team confirms current stock, MOQ and lead time within 24 hours.

Do you support OEM / private label?

Yes. We offer OEM packaging and private-label production for Progesterone Suppository, subject to the regulatory requirements of the destination market.

Which markets have you exported suppositories products to?

We have supplied suppositories products to 50+ countries across Africa, Southeast Asia, Latin America and the Middle East, with experience in ministry-of-health registration and international tenders.

How is the quality of Progesterone Suppository controlled?

Progesterone Suppository is produced in China-GMP workshops (site re-inspected and passed in 2026), released only after full QC testing against BP / enterprise standards, with retained samples kept for one year beyond the product's expiry date.

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