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, sold under the brand name Minocin among others, is a tetracycline antibiotic used to treat a number of bacterial infections such as pneumonia.[2][3] It is generally less preferred than the tetracycline doxycycline.[2][3] It is also used for the treatment of acne and rheumatoid arthritis.[2] It is taken by mouth.[3] Common side effects include nausea, diarrhea, dizziness, allergic react...

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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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