Levofloxacin
- Product NDC
- 70518-0709
- 11-digit product format
- 705180709
- Labeler code
- 70518
- Product ID
- 70518-0709_8bb397f5-8894-349d-e053-2995a90ab3fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076890
- Marketing category
- ANDA
- Marketing start
- 2017-08-22
- 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