Bromostar – DX
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Bromostar - DX
Bromostar-DX Syrup is a combination cough syrup containing Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Chlorpheniramine Maleate. It provides effective relief from dry cough, nasal congestion, throat irritation, and allergic symptoms. The syrup works by suppressing cough reflex, reducing nasal blockage, and relieving allergy-related sneezing or runny nose.
Each 5 ml contains :
Phenylephrine Hydrochloride I.P. 5 mg
Dextromethorphan Hydrobromide I.P. 10 mg
Chlorpheniramine Maleate I.P. 2 mg
Colour : Ponceau 4R
- Dry cough and allergic cough
- Nasal congestion and throat irritation
- Common cold and seasonal allergies
- Relief from sneezing, watery eyes, and runny nose
- As directed by physician.
Medicine Production Process
01
Research & Development (R&D)
New drug molecules are discovered, tested, and optimized for safety, efficacy, and stability.
02
Pre-Formulation Studies
Understanding the drug’s physical, chemical, and biological properties to design the right dosage form.
03
Formulation Development
Creating the final dosage form (tablet, capsule, injection, etc.) with excipients to ensure effectiveness.
04
Raw Material Procurement
High-quality active pharmaceutical ingredients (APIs) and excipients are sourced under strict compliance.
05
Weighing & Dispensing
Precise measurement of raw materials to maintain consistency and quality in every batch.
06
Granulation / Mixing
APIs and excipients are blended or granulated to achieve uniformity for tablet or capsule production.
07
Compression / Filling
The mixture is compressed into tablets or filled into capsules with accuracy.
08
Coating / Finishing
Tablets may be coated for taste masking, controlled release, or product stability.
09
Sterilization (for Injectables)
Parenteral products undergo sterilization to ensure they are safe and free from contaminants.
10
Quality Control (QC) Testing
Each batch is rigorously tested for purity, potency, safety, and compliance with regulatory standards.
11
Packaging
Medicines are packed in blisters, bottles, or sachets with labeling and batch details for traceability.
12
Storage & Distribution
Finished products are stored under controlled conditions and distributed through the pharma supply chain.
