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ParamountParamount Inc. Tokyo, Japan
Tablets

Femotos F

100 mg + 0.35 mg

Iron (III) Hydroxide Polymaltose Complex (eq. to elemental Iron 100 mg) + Folic Acid

Segment 09 · Haematinics · Iron Range

Femotos F100 mg + 0.35 mg

Tablets

Iron (III) Hydroxide Polymaltose Complex (eq. to elemental Iron 100 mg) + Folic Acid

Tablets

Femotos F

100 mg + 0.35 mg

Iron (III) Hydroxide Polymaltose Complex (eq. to elemental Iron 100 mg) + Folic Acid

Iron with folic acid for anaemia in pregnancy and deficiency states.

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

Generic composition
Iron (III) Hydroxide Polymaltose Complex (eq. to elemental Iron 100 mg) + Folic Acid
Strength
100 mg + 0.35 mg
Dosage form
Tablets
Pack sizes
10's & 20's

Other forms & strengths of Femotos F

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.

Femotos F

How it's made

Tablets are made by granulation and compression, then coated where the product calls for it. 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

    Granulation

    The active ingredient and excipients are mixed and granulated so the powder flows and compresses evenly.

  3. 03

    Drying and sizing

    Granules are dried to a set moisture limit and milled to a uniform size.

  4. 04

    Blending

    Lubricant is added and the blend is mixed until the active ingredient is evenly spread through it.

  5. 05

    Compression

    The press forms each tablet to a set weight, hardness and thickness, checked at intervals through the run.

  6. 06

    Coating

    Coated tablets receive a film or sugar coat in a coating pan; uncoated and chewable tablets skip this step.

  7. 07

    Packing

    Tablets are sealed into blister strips, which are coded with the batch number and expiry date.

Batch release tests

  • Uniformity of weight
  • Hardness and friability
  • Disintegration
  • Dissolution
  • Assay of the active ingredient
  • Microbial limits

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