NDC 0555-0171 – Mefloquine Hydrochloride
Mefloquine Hydrochloride 250 mg/1 · Tablet · Oral
Product NDC0555-0171
Product details
- Brand name
- Mefloquine Hydrochloride
- Generic name
- Mefloquine Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076392
- Marketed since
- January 6, 2004
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antimalarial
Active ingredients
- Mefloquine Hydrochloride 250 mg/1
Uses, dosage, side effects and warnings for Mefloquine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0555-0171-78 | 25 BLISTER PACK in 1 CARTON (0555-0171-78) / 1 TABLET in 1 BLISTER PACK (0555-0171-88) | Jan 6, 2004 |
Recalls mentioning this NDC
- D-1396-2012 Jul 4, 2012 · Class II
Tablet Thickness: Product is being recalled due to the potential of being underweight or overweight.
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