Ciprofloxacin
- Product NDC
- 68071-2383
- 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 |
|---|
| 68071-2383-1 | 10 TABLET, COATED in 1 BOTTLE (68071-2383-1) | 2021-04-06 | | No | Historical |
| 68071-2383-2 | 20 TABLET, COATED in 1 BOTTLE (68071-2383-2) | 2021-04-06 | | No | Historical |
| 68071-2383-3 | 30 TABLET, COATED in 1 BOTTLE (68071-2383-3) | 2021-04-06 | | No | Historical |
| 68071-2383-4 | 14 TABLET, COATED in 1 BOTTLE (68071-2383-4) | 2021-04-06 | | No | Historical |
| 68071-2383-8 | 28 TABLET, COATED in 1 BOTTLE (68071-2383-8) | 2021-04-06 | | No | Historical |
| 68071-2383-9 | 90 TABLET, COATED in 1 BOTTLE (68071-2383-9) | 2021-04-06 | | No | Historical |