Levofloxacin
- Product NDC
- 70518-0967
- 11-digit product format
- 705180967
- Labeler code
- 70518
- Product ID
- 70518-0967_8f6f9082-e45f-0101-e053-2a95a90a9709
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076710
- Marketing category
- ANDA
- Marketing start
- 2018-01-19
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record