NDC 67877-0578-30
Minocycline Hydrochloride 45 mg/1 TABLET, FILM COATED, EXTENDED RELEASE
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NDC
67877-0578-30
Generic Name
Minocycline Hydrochloride
Brand Name
Minocycline Hydrochloride
Strength
45 mg/1
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Ascend Laboratories, LLC
FDA Drug Information
Indications & Usage
1 INDICATIONS & USAGE Minocycline hydrochloride extended-release tablets is indicated to treat inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 12 years of age and older. Limitations of Use Minocycline hydrochloride extended-release tablets did not demonstrate any effect on non-inflammatory acne lesions. This formulation of minocycline has not been evaluated in the treatment of infections [see Clinical Studies ( 14 )]. To reduce the development of drug-resistant b…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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