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ferrous sulfate + folic acid

Tablets 200 mg + 0.5 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #21177

This CTD dossier owner and manufacturer, established in the 1980s, operates within South Asia, specializing in the manufacture and supply of pharmaceutical products. Their offerings include tablets, capsules, eye, ear, and nasal drops, as well as oral and injectable suspensions. The company holds EU and US GMP approvals, signifying adherence to high manufacturing standards. Their production lines cater to a diverse range of therapeutic areas, with a focus on infectious diseases, pain management, and ophthalmology. The company boasts a sizable workforce and has a global reach, catering to markets across the world. They are recognized for their commitment to quality, utilizing high-grade chemicals and advanced machinery for production. The company emphasizes its track record in providing quality pharmaceutical products, underscoring its experience in the industry.

Manufacturer usually replies in 2 days

ferrous sulfate

Tablets 325 mg

Dossier type
US CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
FDA
Manufacturer #19316
This pharmaceutical company specializes in both over-the-counter (OTC) and prescription generic drugs, offering products in the form of tablets, capsules, and liquids. Founded in 1992, they initially focused on the US market before expanding globally. They hold a significant distinction as the first Indian company to receive USFDA approvals for producing both OTC and prescription drugs for the US market. Their manufacturing facility is located in India, with a dedicated marketing and distribution center in the USA. Key therapy areas are not specified, nor are details about specific product patents or GMP certifications provided.

Manufacturer usually replies in 19 days

ferrous sulfate + folic acid

Tablets, film coated 500 mg + 0.5 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
India
GMP approvals
WHO
Manufacturer #34549

Established in 2016, this WHO-GMP certified manufacturer specializes in the production and export of pharmaceutical, nutraceutical, and ayurvedic products, including tablets, capsules, syrups, and injections. As a CTD dossier owner and manufacturer, it ensures compliance with international quality standards. The company operates state-of-the-art manufacturing facilities adhering to stringent GMP guidelines. Its products are distributed across multiple countries worldwide, with registrations in regions such as the Dominican Republic, Philippines, Myanmar, Uzbekistan, Turkmenistan, Iraq, and Kuwait. 

 

Manufacturer usually replies in 14 days

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Ferrous Sulfate Heptahydrate Manufacturer

Ferrous Sulfate Heptahydrate belongs to the drug class of Iron products. It is available under the brand names “Fer-In-Sol”, “Feosol”, and “Feratab” among many others. It is mainly a type of iron that is used as a supplement to treat iron deficiency mostly in children and pregnant women. This pharmaceutical medicine has serious interactions with Demeclocycline, Dolutegravir, Fleroxacin, Levofloxacine, and Eltrombopag. It is mostly administered through the oral route in the form of oral liquid, elixir, or tablet. You should tell your doctor or pharmacist before taking iron supplements that contain folic acid if you have vitamin B12 deficiency (pernicious anemia). Vitamin B12 deficiency may be falsely improved by folic acid, but this anemia will not be treated. The lack of vitamin B12, if left untreated, can lead to serious nerve problems, such as numbness, pain, and tingling sensations. It may cause allergic reactions, stomach pain, vomiting, bloody mucous during cough, fever, tarry stools, diarrhea, green-colored stool, constipation, and loss of appetite. It is contraindicated in conditions like gastritis, stomach ulcer, hemolytic anemia, and an overload of iron in the blood. It is highly recommended during pregnancy to cope with anemia and is approved safe by FDA. In lactating women, it is also safe to use and a very small amount of drug is secreted into milk which is harmless to the infant.

How does Ferrous Sulfate Heptahydrate work?

Ferrous Sulfate Heptahydrate provides iron to the body which helps in making healthy red blood cells which in turn carry oxygen to body cells and tissues making them functional.

The cost of Ferrous Sulfate Heptahydrate

For a bulk supply of 100 tablets of Ferrous Sulfate Heptahydrate 325 mg, it costs around 8.66-9.60 dollars. This price may fluctuate from seller to seller.

Sourcing the Ferrous Sulfate Heptahydrate Manufacturers and Suppliers

Navigating our pharmaceutical marketplace

Pipelinepharma being a global B2B pharmaceutical online marketplace, is structured to simplify pharmaceutical deals by providing you with an intuitive interface that is easy to engage with. The selection of Ferrous Sulfate Heptahydrate manufacturers and suppliers can be narrowed down with the use of filters and easily weighed against one another according to medication prices and commercial terms. The advanced filters help you filter out the countries that manufacture this pharmaceutical substance. These also enable you to check the dossier status of this medicine, and the GMP approvals of the different variants of Ferrous Sulfate Heptahydrate. Each manufacturer or supplier product description contains essential information about this substance including clinical data, stability zones, countries where Ferrous Sulfate Heptahydrate is already registered in.

Establishing commercial ties

As a legitimate online pharmaceutical marketplace, Pipelinepharma is a safe and secure B2B platform for drug dealers, wholesalers, and buyers of prescription drugs. An unrestricted number of drugs can be registered and advertised by sellers with a pharmaceutical permit. Sellers, on the other hand, can interact with drug distributors and provide tertiary services directly to the buyers.

Quality assurance

Pipelinepharma evaluates the seller's data during the registration process. The site conducts a product testing operation. As part of their responsibilities, they make sure that each pharmaceutical medicine is free of defects and that its duration of use is validated before they are sold.

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