Levofloxacin
- Product NDC
- 70518-1549
- 11-digit product format
- 705181549
- Labeler code
- 70518
- Product ID
- 70518-1549_94713fd2-a34e-90fb-e053-2995a90ac05d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077438
- Marketing category
- ANDA
- Marketing start
- 2018-10-18
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 750 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record