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ParamountParamount Inc. Tokyo, Japan
Ointment

Neotracin

500 units + 3.5 mg + 5000 IU + 40 mg

Bacitracin + Neomycin Sulphate + Polymyxin B Sulphate + Lidocaine

Segment 11 · Topical Preparations

Neotracin500 units + 3.5 mg + 5000 IU + 40 mg

Ointment

Bacitracin + Neomycin Sulphate + Polymyxin B Sulphate + Lidocaine

Ointment

Neotracin

500 units + 3.5 mg + 5000 IU + 40 mg

Bacitracin + Neomycin Sulphate + Polymyxin B Sulphate + Lidocaine

Topical antibacterial with a local anaesthetic for minor skin infections.

Export fast-track. DRAP export registration in about a month for products developed against export orders. Describe the formulation

Generic composition
Bacitracin + Neomycin Sulphate + Polymyxin B Sulphate + Lidocaine
Strength
500 units + 3.5 mg + 5000 IU + 40 mg
Dosage form
Ointment
Pack sizes
10 gm
Manufacturer
Paramount Pharmaceuticals, Islamabad
Licence
DML 000439 · DRAP GMP
Release
Batch-tested, with Certificate of Analysis

For healthcare professionals. Registration status, brand names and pack presentations vary by market. Experienced a side effect? Report it here.

Neotracin

How it's made

Creams, gels and ointments are made by preparing and emulsifying the bases, then mixing in the active ingredient. Made in the general production section.

How all our dosage forms are made →
  1. 01

    Dispensing

    Each raw material is released by QC, then weighed for the batch under a second person's check.

  2. 02

    Phase preparation

    Oil and water phases are heated and prepared separately.

  3. 03

    Emulsifying

    The phases are combined and homogenised, then the active ingredient is added and evenly mixed.

  4. 04

    Tube filling

    Product is filled into tubes to a set weight and the tubes are crimped and coded.

Batch release tests

  • Fill weight
  • Assay of the active ingredient
  • pH
  • Viscosity and appearance
  • Microbial limits

Limits for this product are on each batch's Certificate of Analysis.