Ciprofloxacin
- Product NDC
- 70518-2202
- 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 |
|---|
| 70518-2202-0 | 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2202-0) | 2019-07-10 | 0000-00-00 | No | Current |
| 70518-2202-1 | 10 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2202-1) | 2019-07-10 | 0000-00-00 | No | Current |
| 70518-2202-2 | 30 TABLET, COATED in 1 BLISTER PACK (70518-2202-2) | 2019-07-11 | 0000-00-00 | No | Current |