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These highlights do not include all the information needed to use MINOCYCLINE HYDROCHLORIDE EXTENDED- RELEASE TABLETS safely and effectively. See full prescribing information for MINOCYCLINE HYDROCHLORIDE EXTENDED-RELEASE TABLETS MINOCYCLINE HYDROCHLORIDE extended-release tablets, for oral use. Initial U.S. Approval: 1971
Medication labelWhy this: Advisory · dailymed-prescription
Minocycline hydrochloride extended-release tablets is indicated to treat only inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 12 years of age and older. Minocycline hydrochloride extended-release tablets did not demonstrate any effect on non-inflammatory acne lesions. Safety of Minocycline hydrochloride extended-release tablets has not been established beyond 12 weeks of use. This formulation of minocycline has not been evaluated in the treatment of infections [see Clinical Studies (14)].To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, Minocycline hydrochloride extended-release tablets should be used only as indicated [see Warnings and Precautions (5.11)].
- generic_name
- minocycline hydrochloride
- product_names
- Minocycline Hydrochloride
- ndc
- 71335-2710, 67877-576, 71335-2710-1
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en