Ciprofloxacin
- Product NDC
- 70518-3417
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK 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 |
|---|
| 70518-3417-0 | 6 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-0) | 2022-05-11 | 0000-00-00 | No | Current |
| 70518-3417-1 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-1) | 2022-05-11 | 0000-00-00 | No | Current |
| 70518-3417-2 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-2) | 2022-05-11 | 0000-00-00 | No | Current |