Mefloquine Hydrochloride 00555-0171
Product NDC
00555-0171- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 6, 2004
- Listing Expires
- December 31, 2027
- Application
- ANDA076392
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Mefloquine Hydrochloride | 250 mg/1 |
Drug Class
Antimalarial [EPC]
Packaging Options(1)
25 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88)