Ofloxacin
- Product NDC
- 68788-8178
- 11-digit product format
- 687888178
- Labeler code
- 68788
- Product ID
- 68788-8178_69703b97-c7b6-4df3-aaa2-465d6669a8d6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ofloxacin
- Dosage form
- SOLUTION
- Route
- OPHTHALMIC
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076513
- Marketing category
- ANDA
- Marketing start
- 2022-04-28
- 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 |
|---|
| 68788-8178-5 | 68788817805 | 1 BOTTLE, DROPPER in 1 CARTON (68788-8178-5) > 5 mL in 1 BOTTLE, DROPPER | 2022-04-28 | 0000-00-00 | No | No | Current |