Moxifloxacin Hydrochloride
- Product NDC
- 71335-2815
- 11-digit product format
- 713352815
- Labeler code
- 71335
- Product ID
- 71335-2815_6ac508d3-c5c6-49b1-ab21-56896601f8ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202632
- Marketing category
- ANDA
- Marketing start
- 2014-03-04
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| C53598599T | MOXIFLOXACIN HYDROCHLORIDE | 186826-86-8 | MOXIFLOXACIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2815-1 | 71335281501 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-2815-1) | 2025-10-15 | No | No | Historical |
| 71335-2815-2 | 71335281502 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2815-2) | 2025-10-15 | No | No | Historical |