Ofloxacin
- Product NDC
- 68788-9204
- 11-digit product format
- 687889204
- Labeler code
- 68788
- Product ID
- 68788-9204_c0bb583b-16dd-4639-b6aa-c0f792514fbb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ofloxacin
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA076622
- Marketing category
- ANDA
- Marketing start
- 2013-05-14
- 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