Ciprofloxacin
- Product NDC
- 70518-2341
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- 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 |
|---|
| 70518-2341-0 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2341-0) | 2019-10-03 | 0000-00-00 | No | Current |
| 70518-2341-3 | 14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2341-3) | 2019-10-20 | 0000-00-00 | No | Current |
| 70518-2341-5 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2341-5) | 2020-05-07 | 0000-00-00 | No | Current |
| 70518-2341-6 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2341-6) | 2020-07-08 | 0000-00-00 | No | Current |