Strength
100 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
57664085385
Classification
Generic
Dosage Form
CAPSULE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
MINOCYCLINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA090867On Market Since
5/13/2013
Pharmacological Classes
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