Ciprofloxacin
- Product NDC
- 68788-7580
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA208921
- Marketing category
- ANDA
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-7580-0 | 6 TABLET, COATED in 1 BOTTLE (68788-7580-0) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7580-1 | 14 TABLET, COATED in 1 BOTTLE (68788-7580-1) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7580-2 | 20 TABLET, COATED in 1 BOTTLE (68788-7580-2) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7580-3 | 30 TABLET, COATED in 1 BOTTLE (68788-7580-3) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7580-4 | 40 TABLET, COATED in 1 BOTTLE (68788-7580-4) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7580-6 | 60 TABLET, COATED in 1 BOTTLE (68788-7580-6) | 2019-12-27 | 0000-00-00 | No | Current |
| 68788-7580-8 | 10 TABLET, COATED in 1 BOTTLE (68788-7580-8) | 2019-12-27 | 0000-00-00 | No | Current |