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 two to four 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 cen...

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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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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)

• ARESTIN Minocycline
• DYNACIN Minocycline
• MINOCIN Minocycline
• MINOCYCLINE 24 discussions
• SOLODYN Minocycline Hydrochloride8 discussions
• VECTRIN Minocycline
• XIMINO Minocycline Hydrochloride