Ciprofloxacin
- Product NDC
- 50090-5483
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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 |
|---|
| 50090-5483-0 | 20 TABLET, COATED in 1 BOTTLE (50090-5483-0) | 2021-03-10 | 0000-00-00 | No | Current |
| 50090-5483-1 | 14 TABLET, COATED in 1 BOTTLE (50090-5483-1) | 2021-03-10 | 0000-00-00 | No | Current |
| 50090-5483-3 | 6 TABLET, COATED in 1 BOTTLE (50090-5483-3) | 2021-03-10 | 0000-00-00 | No | Current |
| 50090-5483-4 | 28 TABLET, COATED in 1 BOTTLE (50090-5483-4) | 2021-03-10 | 0000-00-00 | No | Current |
| 50090-5483-5 | 10 TABLET, COATED in 1 BOTTLE (50090-5483-5) | 2021-03-10 | 0000-00-00 | No | Current |
| 50090-5483-7 | 30 TABLET, COATED in 1 BOTTLE (50090-5483-7) | 2021-03-10 | 0000-00-00 | No | Current |
| 50090-5483-8 | 1 TABLET, COATED in 1 BOTTLE (50090-5483-8) | 2021-03-10 | 0000-00-00 | No | Current |