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Salbutamol Tablets IP/ BP

Salbutamol Tablets IP/ BP

Salbutamol Sulphate | Uncoated Oral Bronchodilator Tablets

Product Composition

IP 2 mg, IP 4 mg and BP 4 mg presentations, each expressed as salbutamol equivalent.

Usage: Prescribed management of reversible bronchospasm.

Category: Respiratory / Antiasthmatic drugs

Categories: Pharmaceutical Exporter India · Pharmaceutical Formulations India · WHO GMP Certified Formulations

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Product Information

Salbutamol Tablets IP/ BP 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

1. Product Introduction

Salbutamol Tablets contain salbutamol sulphate equivalent to 2 mg or 4 mg salbutamol. Salbutamol (albuterol) is a short-acting beta-2 adrenergic agonist bronchodilator used for reversible airway narrowing. These are oral, uncoated tablets, not inhalers. Oral salbutamol generally has a slower onset and more systemic adverse effects than inhaled therapy, so inhaled treatments are usually preferred where suitable. Healthy Life Pharma Pvt. Ltd. and Healthy Inc are the manufacturer/export contacts stated in the supplied brief; verify current authorizations.

2. Product Specifications

StandardLabel strengthPer-tablet compositionDosage form
IP2 mgSalbutamol Sulphate IP equivalent to Salbutamol 2 mg; excipients q.s.Uncoated tablet
IP4 mgSalbutamol Sulphate IP equivalent to Salbutamol 4 mg; excipients q.s.Uncoated tablet
BP4 mgSalbutamol Sulphate BP equivalent to Salbutamol 4 mgUncoated tablet

SKU: Salbutamol Tablets | Therapeutic category: Antiasthmatic / Bronchodilator / Short-acting beta-2 agonist. Packaging and shelf life must be confirmed from the approved label.

3. Manufacturing Technology

For low-dose oral tablets, relevant formulation controls include blend and content uniformity, segregation prevention, compression consistency, disintegration and stability. Suitable manufacturing methods depend on the approved master formula. Specific granulation methods, production equipment and batch capacity have not been independently verified.

4. Quality Assurance

Quality controls may include raw-material identity, assay, uniformity of dosage units, dissolution or disintegration, impurities, microbial quality where applicable, and stability under the relevant IP or BP specification. Acceptance criteria must be taken from the actual registered product specification, not assumed generic limits.

5. Therapeutic Uses

Salbutamol relaxes airway smooth muscle by stimulating beta-2 adrenergic receptors. It may be prescribed for reversible bronchospasm associated with asthma or certain obstructive airway diseases, depending on local approval. Oral salbutamol is not the preferred treatment for a sudden severe asthma attack and should not replace a prescribed rapid-acting inhaler or emergency treatment. It is not an antacid or anti-ulcer medicine.

6. Export and Regulatory Support

For pharmaceutical supply and export enquiries, request current manufacturing licence, GMP evidence, certificates of analysis, stability data, country-specific product registrations and packaging specifications. CTD/ACTD dossiers, COPP, FSC, export destinations and trade terms are subject to documentary confirmation.

7. Frequently Asked Questions

What strengths are listed?

IP 2 mg, IP 4 mg and BP 4 mg uncoated tablets.

Are oral tablets the same as inhalers?

No. Oral tablets act systemically and generally have a slower onset and greater risk of systemic effects such as tremor and palpitations.

Can these tablets treat an acute severe asthma attack?

No. Seek urgent medical care for severe breathlessness; follow the prescribed emergency asthma plan.

Is this an antacid?

No. Salbutamol is a bronchodilator used in respiratory care.

8. Dosage and Administration

Use only on a qualified prescriber’s instructions. Dose and frequency vary with patient age, clinical response, coexisting conditions and local approved labelling. Do not exceed the prescribed dose or use tablets as a substitute for an emergency reliever inhaler. Paediatric dosing requires clinician supervision.

9. Side Effects and Precautions

Possible effects include tremor, nervousness, headache, palpitations, fast heartbeat and muscle cramps. Higher doses may cause low potassium, changes in blood glucose or cardiac rhythm disturbances. Discuss use with a clinician if you have heart disease, arrhythmia, hyperthyroidism, diabetes or take other sympathomimetic medicines. Seek urgent care for worsening breathing, chest pain, fainting or severe allergic symptoms.

10. Storage Instructions

Store in the original packaging, away from excess heat and moisture and out of children’s reach. Follow the exact temperature and expiry instructions on the approved IP or BP pack; a 36-month shelf life or specific storage limit cannot be confirmed from the supplied composition.

For professional and B2B reference only. Prescription requirements, indications, certificates and manufacturing claims depend on current product approvals and documentation.