levofloxacin
- Product NDC
- 42708-063
- 11-digit product format
- 427080063
- Labeler code
- 42708
- Product ID
- 42708-063_b2139693-bcbf-450f-a383-e88523bfc076
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA077652
- Marketing category
- ANDA
- Marketing start
- 2012-11-10
- Marketing end
- 0000-00-00
- Substance
- LEVOFLOXACIN
- Active strength
- 750 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record