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Cabergoline Tablets USP 0,5 mg Ingenus Pharmaceuticals

Ingenus Pharmaceuticals

50,00

In Stock (100 available)

Cabergoline Tablets USP 0,5 mg Ingenus Pharmaceuticals (0,5 mg) — Backed by Ingenus Pharmaceuticals’s commitment to quality, a potent dopamine receptor agonist used to control prolactin levels dur…

100 in stock

This product is for laboratory research use only. Not for human consumption.

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Description

Cabergoline Tablets USP 0,5 mg Ingenus Pharmaceuticals — cabergoline from Ingenus Pharmaceuticals at 0.5 mg. Selective D2 dopamine agonist suppressing pituitary prolactin. Manages prolactin elevation from nandrolone or trenbolone cycles.

Key Benefits

  • Dopamine D2 agonist — suppresses prolactin
  • On-cycle support for nandrolone and trenbolone users
  • Low-dose protocol 0.25 mg twice weekly
  • Pull prolactin at week 6 to confirm dose adequacy
  • Mood elevation and libido support are bonuses
  • Each unit dosed at 5 mg — see Recommended Dosage below for protocol-specific intake

Recommended Dosage

Research dosing: 0.25 mg twice weekly for on-cycle prolactin control with deca or tren. Higher doses (0.5 mg 2×/week) for users with elevated baseline prolactin.

How It Works

Ergot-derived dopamine D2 receptor agonist. Suppresses pituitary prolactin secretion. Clinically used for hyperprolactinemia and Parkinson’s. In AAS protocols: counters the prolactin rise from progestagenic compounds (19-nors).

Pharmacokinetics

Plasma half-life approximately 63–69 hours. Twice-weekly dosing sufficient. Steady-state in 2 weeks.

Potential Side Effects

Nausea common initially — take with food. Orthostatic hypotension possible. High-dose long-term use carries cardiac valve concern (documented in Parkinson’s patients on 3+ mg/day — not at AAS-protocol doses).

Cycle & Stacking Guide

On-cycle support with nandrolone, trenbolone, or progestagenic orals (oxymetholone). 0.25 mg 2×/week throughout cycle. Bloodwork at week 6 — target prolactin <15 ng/mL.

Manufacturer Notes

Ingenus Pharmaceuticals is an independent producer in the research-compound market. Before first use, request the batch-specific Certificate of Analysis and confirm the vial’s tamper-evident seal is intact.

Storage & Handling

Store in the original blister or bottle at 15–25 °C, away from direct sunlight, heat, and humidity. Oral preparations lose potency faster if exposed to moisture; keep the desiccant (if included) with the tablets. Keep out of reach of children. For research and educational purposes only.

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Cabergoline

Physical & Chemical Properties for Research Purposes
Chemical structure of Cabergoline (C26H37N5O2) for laboratory analysis
2D structural representation · PubChem CID 54746 ↗
Chemical Identity
# CAS Registry Number 81409-90-7
Σ IUPAC Name (6aR,9R,10aR)-N-[3-(dimethylamino)propyl]-N-(ethylcarbamoyl)-7-prop-2-enyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
F Molecular Formula C26H37N5O2
M Molecular Weight 451.60 g/mol
SMILES C=CCN1C[C@@H](C[C@@H]2[C@H]1CC3=CNC4=CC=CC2=C34)C(=O)N(CCCN(C)C)C(=O)NCC
InChIKey KORNTPPJEAJQIU-KJXAQDMKSA-N
Melting Point 102-104 °C
Solubility Insoluble in water; soluble in ethanol, chloroform, DMSO
Biological Half-life 63-69 hours (oral)
PubChem CID 54746 ↗
Pharmacological Profile
Aromatization None
Hepatotoxicity Low
Known trade names: Dostinex, Cabaser, Cabergolin

Data sourced from published pharmacological literature and authoritative chemical databases (PubChem, DrugBank, ChEBI). Provided for identification and research reference only.