Ciprofloxacin
- Product NDC
- 68071-5023
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA208921
- Marketing category
- ANDA
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Current FDA listing
- Historical FDA.report record
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-5023-2 | 2 TABLET, COATED in 1 BOTTLE (68071-5023-2) | 2019-08-14 | 0000-00-00 | No | Current |