NDC 71335-2815 – Moxifloxacin Hydrochloride
Moxifloxacin Hydrochloride 400 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2815
Product details
- Brand name
- Moxifloxacin Hydrochloride
- Generic name
- Moxifloxacin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2815-1 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-2815-1) | Oct 15, 2025 |
| 71335-2815-2 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2815-2) | Oct 15, 2025 |
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