Minocycline Hydrochloride 67877-0644
Product NDC
67877-0644- Manufacturer
- Ascend Laboratories, Llc
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 30, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA204453
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Minocycline Hydrochloride | 115 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 (67877-644-01)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-05)
10 BLISTER PACK in 1 CARTON (67877-644-14) / 14 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-644-30)