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ZPHC Cabergoline 0.25mg
ZPHC Cabergoline 0.25mg | Dopamine Receptor Agonist
- Main function: lowers serum prolactin by activating pituitary D₂ receptors, keeping levels in the low-normal range.
- When it’s used: Trenbolone / Nandrolone studies, hyper-prolactinaemia models, libido or erectile-function research.
- Typical research dosing: 0.25 mg twice weekly
(bloodwork-guided ceiling ≈ 1 mg / week). - Expected benefits: prevents gynecomastia, water retention, mood swings, low libido and “tren cough” associated with high prolactin.
- Monitoring advice: track prolactin, blood pressure and mild CNS side-effects (yawning, light-headedness).
- QC: ≥ 99 % API purity (HPLC) • GMP tablet press • tamper-evident cap with scratch-code authenticity.
$66.00
Cabergoline ZPHC — 0.25 mg × 50 tablets
ZPHC Cabergoline 0.25mg is an orally active synthetic ergot derivative containing Cabergoline as its active pharmaceutical ingredient. Functioning as a potent, long-acting, selective dopamine $D_2$ receptor agonist, Cabergoline acts directly upon the $D_2$ receptors of pituitary lactotroph cells to inhibit the synthesis and secretion of prolactin.
Due to its high selectivity for $D_2$ receptors relative to $D_1$, $\alpha_1$, and $\alpha_2$-adrenergic or $5\text{-HT}_1$ and $5\text{-HT}_2$ serotonergic receptors, Cabergoline offers targeted prolactin suppression with an extended elimination half-life (typically 63 to 69 hours), allowing for infrequent dosing schedules while maintaining steady-state prolactin control.
Manufactured by Zhengzhou Pharmaceutical Co., Ltd. (ZPHC) under strict cGMP protocols and verified by analytical batch testing, each tablet delivers a precise 0.25mg dose of pure Cabergoline. Store at controlled room temperature, shielded from direct sunlight, thermal variation, and ambient moisture.
Product Attribute Table
| Attribute | Specification |
| Manufacturer / Brand | ZPHC (Zhengzhou Pharmaceutical Co., Ltd.) |
| Product Name | Cabergoline |
| Active Substance | Cabergoline (Dostinex) |
| Chemical Name | 1-[(6-allylergolin-8$\beta$-yl)carbonyl]-1-[3-(dimethylamino)propyl]-3-ethylurea |
| Dosage / Concentration | 0.25 mg/tablet |
| Form | Oral Tablet |
| Compound Category | Dopamine $D_2$ Receptor Agonist / Prolactin Inhibitor |
| Storage Requirements | Controlled Room Temperature (15°C – 25°C), Protect strictly from light and ambient moisture |
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