NDC 70771-1167-0
minocycline hydrochloride 135 mg/1
minocycline hydrochloride · TABLET, EXTENDED RELEASE
minocycline hydrochloride is a tablet, extended release containing minocycline hydrochloride at a strength of 135 mg/1. Manufactured by Zydus Lifesciences Limited.
Key Facts
- Brand Name
- minocycline hydrochloride
- Generic Name
- minocycline hydrochloride
- NDC Code (Package)
70771-1167-0- NDC Code (Product)
70771-1167- Manufacturer
- Zydus Lifesciences Limited
- Strength
- 135 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA203553
- Marketing Start
- 03/07/2018
Recall History
No Recall HistoryView Full Drug Page
minocycline hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.