Ciprofloxacin
- Product NDC
- 68071-2384
- 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 |
|---|
| 68071-2384-1 | 10 TABLET, COATED in 1 BOTTLE (68071-2384-1) | 2021-04-09 | | No | Historical |
| 68071-2384-2 | 20 TABLET, COATED in 1 BOTTLE (68071-2384-2) | 2021-04-09 | | No | Historical |
| 68071-2384-3 | 30 TABLET, COATED in 1 BOTTLE (68071-2384-3) | 2021-04-09 | | No | Historical |
| 68071-2384-4 | 14 TABLET, COATED in 1 BOTTLE (68071-2384-4) | 2021-04-09 | | No | Historical |
| 68071-2384-5 | 15 TABLET, COATED in 1 BOTTLE (68071-2384-5) | 2021-04-09 | | No | Historical |
| 68071-2384-6 | 60 TABLET, COATED in 1 BOTTLE (68071-2384-6) | 2021-04-09 | | No | Historical |
| 68071-2384-7 | 21 TABLET, COATED in 1 BOTTLE (68071-2384-7) | 2021-04-09 | | No | Historical |
| 68071-2384-8 | 28 TABLET, COATED in 1 BOTTLE (68071-2384-8) | 2021-04-09 | | No | Historical |
| 68071-2384-9 | 90 TABLET, COATED in 1 BOTTLE (68071-2384-9) | 2021-04-09 | | No | Historical |