Minocycline Hydrochloride 70771-1138
Product NDC
70771-1138- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 7, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA203553
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Minocycline Hydrochloride | 45 mg/1 |
Drug Class
Decreased Prothrombin Activity [PE]Tetracycline-class Drug [EPC]Tetracyclines [CS]
Packaging Options(6)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1138-0)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1138-1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1138-3)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1138-5)
10 BLISTER PACK in 1 CARTON (70771-1138-7) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1138-9)