Levofloxacin
- Product NDC
- 68788-9707
- 11-digit product format
- 687889707
- Labeler code
- 68788
- Product ID
- 68788-9707_c6de4ad6-2321-467e-a6d9-7cc1781c3028
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA201043
- Marketing category
- ANDA
- Marketing start
- 2011-08-12
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record