Moxifloxacin
- Product NDC
- 50090-6357
- 11-digit product format
- 500906357
- Labeler code
- 50090
- Product ID
- 50090-6357_820f6616-7ce5-4adf-8515-21efd5b02997
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA202867
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 5 mg/mL
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6357-0 | 50090635700 | 1 BOTTLE in 1 CARTON (50090-6357-0) / 3 mL in 1 BOTTLE | 1 bottle | 2023-02-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Moxifloxacin | A-S Medication Solutions | 2023-04-19 | HUMAN PRESCRIPTION DRUG LABEL | 5 |