Ofloxacin
- Product NDC
- 68788-0617
- 11-digit product format
- 687880617
- Labeler code
- 68788
- Product ID
- 68788-0617_12dbdcde-3e5f-48b4-a063-c91b98989d53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ofloxaxin
- Dosage form
- SOLUTION/ DROPS
- Route
- AURICULAR (OTIC)
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA076616
- Marketing category
- ANDA
- Marketing start
- 2013-03-22
- Marketing end
- 0000-00-00
- Substance
- OFLOXACIN
- Active strength
- 3 mg/mL
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record