Moxifloxacin
- Product NDC
- 72162-2107
- 11-digit product format
- 721622107
- Labeler code
- 72162
- Product ID
- 72162-2107_5e65bcf7-98de-4ec2-adf9-cbb8ec0bbe68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090080
- Marketing category
- ANDA
- Marketing start
- 2017-07-01
- Substance
- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
- 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 |
|---|
| B8956S8609 | MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE | 192927-63-2 | MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE |
| U188XYD42P | MOXIFLOXACIN | 151096-09-2 | moxifloxacin |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2107-2 | 72162210702 | 1 BOTTLE, DROPPER in 1 CARTON (72162-2107-2) / 3 mL in 1 BOTTLE, DROPPER | 2017-07-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Moxifloxacin | Bryant Ranch Prepack | 2024-10-04 | HUMAN PRESCRIPTION DRUG LABEL | 101 |