Ofloxacin
- Product NDC
- 68788-8264
- 11-digit product format
- 687888264
- Labeler code
- 68788
- Product ID
- 68788-8264_34e7949c-af52-4836-a68d-c74df99a89c0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078559
- Marketing category
- ANDA
- Marketing start
- 2022-09-26
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8264-5 | 68788826405 | 1 BOTTLE, PLASTIC in 1 CARTON (68788-8264-5) > 5 mL in 1 BOTTLE, PLASTIC | 2022-09-26 | 0000-00-00 | No | No | Current |