Minocycline Hydrochloride 57664-0852
Product NDC
57664-0852- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 13, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA090867
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Minocycline Hydrochloride | 75 mg/1 |
Drug Class
Decreased Prothrombin Activity [PE]Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(2)
500 CAPSULE in 1 BOTTLE (57664-852-13)
100 CAPSULE in 1 BOTTLE (57664-852-88)