Ciprofloxacin
- Product NDC
- 68071-2404
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA208921
- Marketing category
- ANDA
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-2404-2 | 2 TABLET, COATED in 1 BOTTLE (68071-2404-2) | 2021-05-21 | | No | Historical |
| 68071-2404-4 | 4 TABLET, COATED in 1 BOTTLE (68071-2404-4) | 2021-05-21 | | No | Historical |
| 68071-2404-6 | 6 TABLET, COATED in 1 BOTTLE (68071-2404-6) | 2021-05-21 | | No | Historical |