Export: +91 9820402906   Domestic: +91 7710003340 | HR: +91 9137757219
Prazosin Tablets IP

Prazosin Tablets IP

Composition: Prazosin Hydrochloride IP equivalent to Prazosin 2 mg, 2.5 mg or 5 mg per tablet.

Dosage form: Film-coated tablet

Therapeutic category: Antihypertensive / Selective alpha-1 adrenergic blocker

Usage: Management of high blood pressure as prescribed.

Manufacturer (as supplied): Healthy Life Pharma Pvt. Ltd.

Exporter (as supplied): Healthy Inc

SKU: Prazosin Tablets

Product Information

Prazosin Tablets IP 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.

Description

Categories: Contract Manufacturer · Formulations Exporter India · Manufacturing Pharmaceutical Company India · Pharmaceutical Exporter India · Pharmaceutical Formulations India · Tablets Manufacturer · WHO GMP Certified Formulations

1. Product Introduction

Prazosin is a selective alpha-1 adrenergic receptor antagonist used to manage hypertension. It relaxes blood vessels, reducing peripheral vascular resistance and blood pressure. Healthy Life Pharma Pvt. Ltd. is identified as manufacturer and Healthy Inc as exporter in the supplied information. Manufacturing authorizations and certifications should be verified against current documents.

2. Product Specifications

Product namePrazosin Tablets IP
Active ingredientPrazosin Hydrochloride IP, equivalent to Prazosin
Strengths2 mg / 2.5 mg / 5 mg
Dosage formFilm-coated tablets
Pharmacopoeial standardIP (as supplied)
Therapeutic classAntihypertensive / Alpha-1 blocker
SKUPrazosin Tablets
Packaging / shelf lifeTo be confirmed against approved product specifications

Available compositions

VariantComposition per film-coated tablet
2 mgPrazosin Hydrochloride IP equivalent to Prazosin 2 mg
2.5 mgPrazosin Hydrochloride IP equivalent to Prazosin 2.5 mg; excipients q.s.
5 mgPrazosin Hydrochloride IP equivalent to Prazosin 5 mg; excipients q.s.

1 mg and extended-release (XL) variants mentioned in general marketing copy are not confirmed in the supplied composition list and are not presented as available products.

3. Manufacturing Considerations

Low-strength formulations require validated blending, content-uniformity controls, suitable film coating and controlled production conditions. Actual processes, including granulation methods and moisture-control measures, depend on the approved manufacturing dossier and site capabilities. Specific technology claims require documentation.

4. Quality Assurance

Relevant release and stability testing may include identification, assay, content uniformity, dissolution, impurities, microbial quality where applicable and packaging integrity, according to the approved IP specification and registered dossier. No universal assay or dissolution limit is claimed here without product-specific documentation.

5. Mechanism and Therapeutic Uses

Prazosin blocks postsynaptic alpha-1 receptors, causing vasodilation and lowering blood pressure. Its principal indication in this listing is hypertension. Other uses, such as benign prostatic hyperplasia, Raynaud phenomenon or PTSD-associated nightmares, depend on local approvals and clinical guidance and should not be treated as approved indications for this product without confirmation.

6. Export and Regulatory Support

For B2B enquiries, partners may request current manufacturing licenses, GMP evidence, certificates of analysis, product dossiers, stability information and export documentation where available. CTD/ACTD, COPP, FSC, shipment terms and market registrations are subject to verification and applicable national requirements.

7. Frequently Asked Questions

What strengths are listed?

2 mg, 2.5 mg and 5 mg, each as a film-coated IP tablet.

What is prazosin used for?

It is an alpha-1 blocker prescribed to treat high blood pressure.

Why is the first dose important?

Prazosin may cause a pronounced fall in blood pressure, dizziness or fainting when starting therapy or increasing the dose. Follow the prescriber's specific instructions.

Are private-label or export services available?

Contact the company to confirm current capacity, regulatory authorization and market-specific documentation.

8. Dosage and Administration

Prescription medicine: Dose and titration must be individualized by the treating clinician. Starting doses are generally low because of the risk of first-dose syncope and orthostatic hypotension. Do not start, stop, restart or change the dose without medical advice. Follow the approved local prescribing information.

9. Side Effects and Precautions

  • First-dose syncope and orthostatic hypotension: Dizziness, fainting or falls can occur, especially after the first dose or dose escalation.
  • Other effects: Headache, fatigue, palpitations, drowsiness and nasal congestion may occur.
  • Interactions: Other blood-pressure-lowering medicines and PDE5 inhibitors such as sildenafil may increase hypotension risk.
  • Safety: Rise slowly from sitting or lying positions; avoid driving if dizzy. Seek urgent care for fainting, severe weakness, chest pain or other serious symptoms.
  • Medical review: Pregnancy, breastfeeding, kidney/liver conditions and concurrent medicines require professional assessment.

This content is informational and is not a substitute for the approved package insert or professional medical advice.

10. Storage Instructions

Store in the original packaging, protected from moisture and light, at the temperature specified on the approved product label. Keep out of reach of children. Exact storage temperature and shelf life must be verified against approved stability data.