Levaquin
- Product NDC
- 70518-0501
- 11-digit product format
- 705180501
- Labeler code
- 70518
- Product ID
- 70518-0501_85845d1a-2f50-6f79-e053-2991aa0afcd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020634
- Marketing category
- NDA
- Marketing start
- 2017-05-09
- 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