Minocycline Hydrochloride 65862-0885
Product NDC
65862-0885- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 13, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA202261
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Minocycline Hydrochloride | 105 mg/1 |
Drug Class
Decreased Prothrombin Activity [PE]Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(4)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-01)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-05)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-30)
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-885-99)