Ofloxacin
- Product NDC
- 68788-8993
- 11-digit product format
- 687888993
- Labeler code
- 68788
- Product ID
- 68788-8993_13222bcc-2b0c-46bb-91a6-574c95221cee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078559
- Marketing category
- ANDA
- Marketing start
- 2016-02-15
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8993-5 | 68788899305 | 5 mL in 1 BOTTLE, PLASTIC (68788-8993-5) | 5 ml | 2016-02-15 | 0000-00-00 | No | No | Current |