NDC 57237-156 – Moxifloxacin Hydrochloride
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC57237-156
Product details
- Brand name
- Moxifloxacin Hydrochloride
- Generic name
- Moxifloxacin Hydrochloride
- Labeler
- Rising Pharma Holdings, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202632
- Marketed since
- March 4, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Fluoroquinolone Antibacterial
Active ingredients
- Moxifloxacin Hydrochloride 400 mg/1
Uses, dosage, side effects and warnings for Moxifloxacin Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 57237-156-30 | 30 TABLET, FILM COATED in 1 BOTTLE (57237-156-30) | Mar 4, 2014 |
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