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Dextromethorphan Hbr + Guaiphenesin + Chlorpheniramine Maleate + Ammonium Chloride

CATEGORY : Allopathy



STRENGTH : 5mg + 50mg + 2.5mg + 60mg


LABEL CLAIM : Each 5ml contains Dextromethorphan Hbr IP 5mg + Guaiphenesin IP 50mg + Chlorpheniramine Maleate IP 2.5mg + Ammonium Chloride IP 60mg


Price : ₹0.00 /
2000 Available
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  • Brand Name (If already marketed)
    Mfg. Formula (Qualitative / Quantative) Avaliable
    Brief manufacturing process (Flow chart) Avaliable
    Manufacturing cycle time (Mfg lead time) 25 Days
    Minimum & Maximum commercial batch size 500 Ltr - 2000 Ltr (5000 Botlles to 20000 Bottles)
    Annual capacity 200000 Bottles
    List of Equipment's Avaliable
    Process Validation Report for review (In case PV already completed) Avaliable
    Process controls (CPP) Avaliable
    Executed BMR and BPR for review Avaliable
    Stability data in final pack (Long Term/intermediate/Accelerated)
    B.Size of stability batches
    B.Size Scale-Up capacity
    In-vitro release profile : (If applicable) Avaliable
    Innovator or Competitor Brand name (Used as reference) Avaliable
    Media-1 (Field)
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    Media-5 (Field)
    BE / CT study  report (If applicable) Avaliable
    Scale Up and Process Validation report Avaliable
    MSDS Avaliable
    Shelf life of the product in company letterhead Avaliable
  • Vendor details for Active Ingredients Avaliable
    Pharmacopoeial status
    Specification (s) Avaliable
    Valid Reference standard/Working standard availability with CoA Avaliable
    Valid Impurity standard availability with CoA Avaliable
    Critical Quality Attribute (If any) Avaliable
    Excipient vendor details Avaliable
  • Active Ingredients Specification Avaliable
    Excipients Specification Avaliable
    In-process / Bulk Specification Avaliable
    Finished Product Specification Avaliable
    Shelf Life Specification Avaliable
    Active Ingredients Method Of Analysis Avaliable
    Excipients Method Of Analysis Avaliable
    In-process / Bulk Method Of Analysis Avaliable
    Finished Product Method Of Analysis Avaliable
    Shelf Life Method Of Analysis Avaliable
    Three batch samples (Acc/Near Exp/Fresh)in final pack (Equivalent of two times of complete analysis) Avaliable
    If Partner / Customer want to do joint analysis, will you provide suitable dates? Avaliable
  • Blend / Bulk Assay Method Avaliable
    FP / Stability Assay Method Avaliable
    Related Substances (Impurities) Avaliable
    Uniformity Of Dosage Units Avaliable
    Dissolution Avaliable
    Res Solv (OVI) Avaliable
    Preservative content
    Heavy metals Avaliable
    Identification Test Avaliable
    Others (If any) Avaliable
  • Manufacturing license with validity Avaliable
    Manufacturing license number Avaliable
    Location license (form 25, form 28 In case of India) Avaliable
    Stability Data Avaliable
    Long Term Stability Data (In Months)
    Accelerated Stability Data (In Months)
  • If Partner / Customer want to do Quality and Facility audit, will you provide suitable dates? Avaliable
    Launch period of the product (Lead Time)
  • Generic Name Avaliable
    Dosage form Avaliable
    Label Claim (With special ingredients if added in the formulation) Avaliable
    Colours Avaliable
    Details of pack- Pack size and Type of pack Avaliable
    Warning as per DCGI Avaliable
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    Storage condition and shelf life Avaliable
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    Packing material: Layouts, mock-ups (Sales and PS), leaflet in editable form. Avaliable
    Mfg. Address Avaliable
    Any other text matter for printing Avaliable
    List of approved vendors Avaliable
  • Any Other Details : (Except above mentioned)

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