Ciprofloxacin
- Product NDC
- 68071-3901
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofolxacin
- Dosage form
- TABLET
- 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 |
|---|
| 68071-3901-1 | 100 TABLET in 1 BOTTLE (68071-3901-1) | 2025-10-14 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | NuCare Pharmaceuticals,Inc. | 2025-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 1 |