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Prednisone (Prednisone)

Trade Name : PredniSONE

West-Ward Pharmaceuticals Corp.

TABLET

Strength 10 mg/1

PREDNISONE Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

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Product information is meant for

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Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Prednisone (Prednisone) which is also known as PredniSONE and Manufactured by West-Ward Pharmaceuticals Corp.. It is available in strength of 10 mg/1 per ml. Read more

Prednisone (Prednisone) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • Prednisone Tablets USP are available for oral administration containing either 1 mg, 2.5 mg, 5 mg, 10 mg, 20 mg or 50 mg of prednisone USP. Each tablet contains the following inactive ingredients: lactose monohydrate, magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium starch glycolate and stearic acid (1 mg, 2.5 mg, and 5 mg only).
  • Prednisone Oral Solution USP is formulated for oral administration containing 5 mg per 5 mL of prednisone USP and alcohol 5%. The oral solution contains the following inactive ingredients: anhydrous citric acid, edetate disodium, fructose, hydrochloric acid, maltol, peppermint oil, polysorbate 80, propylene glycol, saccharin sodium, sodium benzoate, vanilla flavor and purified water.
  • Prednisone Oral Solution (Concentrate) is formulated for oral administration containing 5 mg per mL of prednisone USP and alcohol 30%. In addition, the oral solution contains the following inactive ingredients: anhydrous citric acid, poloxamer 188, propylene glycol and purified water.
  • Prednisone tablets contain prednisone which is a glucocorticoid. Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. The chemical name for prednisone is 17,21-dihydroxypregna-1,4-dienne-3,11,20-trione. The structural formula is represented below:
  • CHO M.W. 358.44
  • Prednisone is a white to partially white, crystalline powder. It is very slightly soluble in water; slightly soluble in alcohol, chloroform, dioxane, and methanol.
  • Naturally occurring glucocorticoids (hydrocortisone and cortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Their synthetic analogs are primarily used for their potent anti-inflammatory effects in disorders of many organ systems.
  • Glucocorticoids cause profound and varied metabolic effects. In addition, they modify the bodyu2019s immune responses to diverse stimuli.
  • Prednisone tablets and solutions are indicated in the following conditions:
  • Prednisone tablets and oral solutions are contraindicated in systemic fungal infections and known hypersensitivity to components.
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  • The following adverse reactions have been reported with prednisone or other corticosteroids:
  • Gastric irritation may be reduced if taken before, during, or immediately after meals or with food or milk.
  • The maximal activity of the adrenal cortex is between 2 am and 8 am, and it is minimal between 4 pm and midnight. Exogenous corticosteroids suppress adrenocorticoid activity the least when given at the time of maximal activity (am) for single dose administration. Therefore, it is recommended that prednisone be administered in the morning prior to 9 am and when large doses are given, administration of antacids between meals to help prevent peptic ulcers. Multiple dose therapy should be evenly distributed in evenly spaced intervals throughout the day.
  • Dietary salt restriction may be advisable in patients.
  • Do not stop taking this medicine without first talking to your doctor. Avoid abrupt withdraw of therapy.
  • The initial dosage of prednisone may vary from 5 mg to 60 mg per day, depending on the specific disease entity being treated. In situations of less severity lower doses will generally suffice, while in selected patients higher initial doses may be required. The initial dosage should be maintained or adjusted until a satisfactory response is noted. If after a reasonable period of time there is a lack of satisfactory clinical response, prednisone should be discontinued and the patient transferred to other appropriate therapy. After a favorable response is noted, the proper maintenance dosage should be determined by decreasing the initial drug dosage in small increments at appropriate time intervals until the lowest dosage which will maintain an adequate clinical response is reached. It should be kept in mind that constant monitoring is needed in regard to drug dosage. Included in the situations which may make dosage adjustments necessary are changes in clinical status secondary to remissions or exacerbations in the disease process, the patientu2019s individual drug responsiveness, and the effect of patient exposure to stressful situations not directly related to the disease entity under treatment; in this latter situation, it may be necessary to increase the dosage of prednisone for a period of time consistent with the patientu2019s condition. If after long-term therapy the drug is to be stopped, it recommended that it be withdrawn gradually rather than abruptly.
  • PredniSONE Tablets USP
  • 1 mg u2013 White to off-white, round, biconvex tablet; scored on one side and product identification u201c54 [above] 092u201d debossed on the other side.
  • NDC 0054-8739-25: 10x10 Unit-Dose
  • NDC 0054-4741-25: Bottle of 100 Tablets
  • NDC 0054-4741-31: Bottle of 1,000 Tablets
  • 2.5 mg u2013 White to off-white, round, biconvex tablet; scored on one side and product identification u201c54 [above] 339u201d debossed on the other side.
  • NDC 0054-8740-25: 10x10 Unit-Dose
  • NDC 0054-4742-25: Bottle of 100 Tablets
  • 5 mg u2013 White to off-white, round, biconvex tablet; scored on one side and product identification u201c54 [above] 612u201d debossed on the other side.
  • NDC 0054-8724-25: 10x10 Unit-Dose
  • NDC 0054-4728-25: Bottle of 100 Tablets
  • NDC 0054-4728-31: Bottle of 1,000 Tablets
  • 10 mg u2013 White to off-white, round, biconvex tablet; scored on one side and product identification u201c54 [above] 899u201d debossed on the other side.
  • NDC 0054-0017-20: 10x10 Unit-Dose
  • NDC 0054-0017-25: Bottle of 100 Tablets
  • NDC 0054-0017-29: Bottle of 500 Tablets
  • 20 mg u2013 White to off-white, round, biconvex tablet; scored on one side and product identification u201c54 [above] 760u201d debossed on the other side.
  • NDC 0054-0018-20: 10x10 Unit-Dose
  • NDC 0054-0018-25: Bottle of 100 Tablets
  • NDC 0054-0018-29: Bottle of 500 Tablets
  • 50 mg u2013 White to off-white, round, biconvex tablet; scored on one side and product identification u201c54 [above] 343u201d debossed on the other side.
  • NDC 0054-0019-20: 10x10 Unit-Dose
  • NDC 0054-0019-25: Bottle of 100 Tablets
  • Store at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F). [See USP Controlled Room Temperature.]
  • Dispense in a tight, child-resistant container as defined in the USP/NF.
  • PROTECT FROM MOISTURE.
  • PredniSONE Oral Solution USP, 5 mg per 5 mL
  • Clear, colorless, slightly viscous solution.
  • NDC 0054-3722-50: Bottle of 120 mL
  • NDC 0054-3722-63: Bottle of 500 mL
  • Store at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F). [See USP Controlled Room Temperature.]
  • Dispense in a tight, light-resistant, child-resistant container as defined in the USP/NF.
  • PredniSONE Oral Solution (Concentrate), 5 mg per mL
  • Clear, colorless, slightly viscous solution.
  • NDC 0054-3721-44: Bottle of 30 mL with calibrated dropper (graduations of 0.25 mL [1.25 mg] to 1 mL [5 mg] on the dropper)
  • Store at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F). [See USP Controlled Room Temperature.]
  • Dispense only in the bottle and only with the calibrated dropper provided.
  • Discard opened bottle after 90 days.
  • Distr. by: n
  • Pharmaceuticals Corp.
  • Eatontown, NJ 07724
  • Revised November 2017
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Validated Cold Chain Shipment

Validated Cold Chain Shipment

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