Minolira

Active Ingredient(s): Minocycline Hydrochloride
FDA Approved: * May 8, 2017
Pharm Company: * DR REDDYS LABS LTD
Category: Antibiotics

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Minolira Overview

Minocycline is a broad-spectrum tetracycline antibiotic, and has a broader spectrum than the other members of the group. It is a bacteriostatic antibiotic, classified as a long-acting type. As a result of its long half-life it generally has serum levels 2–4 times that of the simple water-soluble tetracyclines. Minocycline is the most lipid-soluble of the tetracycline-class antibiotics, giving it the greatest penetration into the prostate and brain, but also the greatest amount of centra...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Minocycline

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Possible Dosages for this and Related Drugs:

Minocycline Hydrochloride
  • Capsule: 100mg, 50mg, 75mg
  • Capsule, Extended Release: 112.5mg, 135mg, 45mg, 67.5mg, 90mg
  • Injection: 100mg, 100mg/vial
  • Powder, Extended Release: 1mg
  • Suspension: 50mg/5ml
  • Tablet: 100mg, 135mg, 45mg, 50mg, 75mg, 90mg
  • Tablet, Extended Release: 105mg, 115mg, 135mg, 45mg, 55mg, 65mg, 80mg, 90mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Minolira: (2 results)

Sorted by National Drug Code
  • 43598-539 Minolira 135 mg Oral Tablet, Extended Release by Dr. Reddys Laboratories Inc
  • 43598-540 Minolira 105 mg Oral Tablet, Extended Release by Dr. Reddys Laboratories Inc

Other drugs which contain Minocycline Hydrochloride or a similar ingredient: (7 results)





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