Moxifloxacin
- Product NDC
- 50090-3147
- 11-digit product format
- 500903147
- Labeler code
- 50090
- Product ID
- 50090-3147_f439467b-6b2b-4eb0-8ad2-5668f0a1e1fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Moxifloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076938
- Marketing category
- ANDA
- Marketing start
- 2014-03-05
- Marketing end
- 0000-00-00
- Substance
- MOXIFLOXACIN HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 50090-3147-0 | 50090314700 | 10 TABLET, FILM COATED in 1 BOTTLE (50090-3147-0) | 2019-04-25 | 0000-00-00 | No | No | Current |
| 50090-3147-1 | 50090314701 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3147-1) | 2017-10-02 | 0000-00-00 | No | No | Current |