Ciprofloxacin
- Product NDC
- 68071-3693
- 11-digit product format
- 680713693
- Labeler code
- 68071
- Product ID
- 68071-3693_238284a8-b38f-82af-e063-6394a90a79e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofolxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2023-10-01
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4BA73M5E37 | CIPROFLOXACIN HYDROCHLORIDE | 86393-32-0 | CIPROFLOXACIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3693-6 | 68071369306 | 6 TABLET in 1 BOTTLE (68071-3693-6) | 6 tablet | 2024-10-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | NuCare Pharmaceuticals, Inc. | 2024-10-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |