Moxifloxacin
- Product NDC
- 72789-233
- 11-digit product format
- 727890233
- Labeler code
- 72789
- Product ID
- 72789-233_40ad11b9-8248-8d3f-e063-6294a90a26eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA076938
- Marketing category
- ANDA
- Marketing start
- 2014-03-05
- 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 |
| U188XYD42P | MOXIFLOXACIN | 151096-09-2 | Moxifloxacin |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-233-10 | 72789023310 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-233-10) | 2022-02-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Moxifloxacin | PD-Rx Pharmaceuticals, Inc. | 2025-10-08 | HUMAN PRESCRIPTION DRUG LABEL | 21 |
| Moxifloxacin | PD-Rx Pharmaceuticals, Inc. | 2024-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 20 |