
Composition: Each sugar-coated tablet contains Methylergonovine Maleate IP or USP 0.125 mg.
Usage: Control of uterine bleeding following childbirth under medical supervision.
Category: Generic Drugs and Medicine
Therapeutic category: Uterotonic / Ergot alkaloid
Manufacturer: Healthy Life Pharma Pvt. Ltd. (as supplied; WHO-GMP status to be verified)
Exporter: Healthy Inc (as supplied)
SKU: Methyl Ergonovine Tablets
Methylergonovine Maleate Tablets is listed for pharmaceutical business-to-business enquiries. Exact active ingredients, formulation, strength, pack configuration and manufacturer details should be confirmed against the product label and approved technical documentation before ordering.
Methylergonovine maleate (also called methylergometrine maleate) is an ergot-derived uterotonic used under medical supervision to help manage uterine atony and bleeding following childbirth, as indicated in the locally approved product label. It increases uterine smooth-muscle tone and contractions. Oral tablets are not a substitute for emergency treatment of severe postpartum hemorrhage.
Healthy Life Pharma Pvt. Ltd. is identified as the manufacturer and Healthy Inc as the exporter in the supplied product information. Certification and supply claims require documentary verification.
| Product | Methylergonovine Maleate Tablets |
|---|---|
| Composition | Methylergonovine Maleate IP 0.125 mg or USP 0.125 mg per tablet |
| Strength | 0.125 mg (125 micrograms) |
| Dosage form | Sugar-coated tablet |
| Therapeutic class | Uterotonic / Ergot alkaloid |
| Use | Clinician-directed control of uterine bleeding after delivery, according to approved indications |
| Pharmacopoeial grade | IP or USP, as stated on the individual label |
| Packaging / shelf life | To be verified against approved label and stability data |
| SKU | Methyl Ergonovine Tablets |
Because each tablet contains only 125 micrograms of active ingredient, manufacturing requires carefully validated blending and content-uniformity controls. Protection from light and suitable packaging may be important depending on stability studies. Specific low-actinic processing, coating techniques, refrigeration and production equipment are not confirmed by the supplied product information.
Quality testing should follow the applicable approved IP or USP monograph and product specifications, including identification, assay, content uniformity, dissolution where applicable, related substances and stability. Specific numerical release limits and validated methods must be taken from the applicable monograph or approved dossier rather than assumed.
Methylergonovine produces increased uterine tone and contractions through actions on uterine smooth muscle and related receptor pathways. It may be prescribed after delivery to support uterine involution and manage uterine bleeding, depending on local authorization and clinical circumstances. It can also constrict blood vessels and markedly raise blood pressure.
Not for labor induction or use before delivery. Acute major postpartum hemorrhage requires immediate emergency obstetric management.
Potential B2B support may include product dossiers, certificates of analysis, stability information and export documentation, subject to actual availability and destination-country requirements. WHO-GMP certification, COPP, FSC, registration, export permissions and market authorization should be verified before making commercial claims.
Q: What strength is supplied?
A: 0.125 mg (125 micrograms) per sugar-coated tablet, in IP and USP-labelled variants.
Q: Can it be used to start labor?
A: No. It must not be used before delivery to induce or augment labor.
Q: Is it safe in high blood pressure?
A: Hypertension and preeclampsia/eclampsia are important contraindications because the medicine can cause dangerous vasoconstriction.
Q: What about breastfeeding?
A: Methylergonovine may affect milk production and expose the infant. Follow the exact product label and clinician guidance; some labels advise avoiding breastfeeding during treatment and for at least 12 hours after the last dose.
Oral dosing and duration must be prescribed by an obstetric clinician according to the specific approved 0.125 mg product label. Regimens for other strengths, including 0.2 mg products, should not be transferred to this tablet without checking the local label. Do not self-administer for heavy bleeding or substitute oral therapy for emergency care.
Protect from light and moisture and store according to the approved label for the specific IP or USP tablet. Refrigeration and a particular temperature range must not be assumed without validated product stability information.