Moxifloxacin
- Product NDC
- 68788-7404
- 11-digit product format
- 687887404
- Labeler code
- 68788
- Product ID
- 68788-7404_72097856-9b88-4fbe-acf3-3a2ecffa17a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- moxifloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090080
- Marketing category
- ANDA
- Marketing start
- 2018-06-11
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE MONOHYDRATE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7404-3 | 68788740403 | 1 BOTTLE, DROPPER in 1 CARTON (68788-7404-3) > 3 mL in 1 BOTTLE, DROPPER | 2018-06-11 | 0000-00-00 | No | No | Current |