Ciprofloxacin
- Product NDC
- 68071-2510
- 11-digit product format
- 680712510
- Labeler code
- 68071
- Product ID
- 68071-2510_ca3c95bc-e11c-07d3-e053-2a95a90a287b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Quinolone Antimicrobial [EPC],Quinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4BA73M5E37 | CIPROFLOXACIN HYDROCHLORIDE | 86393-32-0 | CIPROFLOXACIN HYDROCHLORIDE |
| 5E8K9I0O4U | CIPROFLOXACIN | 85721-33-1 | Ciprofloxacin |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2510-1 | 68071251001 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-2510-1) | 2021-08-23 | 0000-00-00 | No | No | Current |
| 68071-2510-2 | 68071251002 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-2510-2) | 2021-08-23 | 0000-00-00 | No | No | Current |
| 68071-2510-3 | 68071251003 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-2510-3) | 2021-08-23 | 0000-00-00 | No | No | Current |
| 68071-2510-4 | 68071251004 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-2510-4) | 2021-08-23 | 0000-00-00 | No | No | Current |
| 68071-2510-6 | 68071251006 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-2510-6) | 2021-08-23 | 0000-00-00 | No | No | Current |
| 68071-2510-8 | 68071251008 | 28 TABLET, FILM COATED in 1 BOTTLE (68071-2510-8) | 2021-08-23 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | NuCare Pharmaceuticals,Inc. | 2021-08-23 | HUMAN PRESCRIPTION DRUG LABEL | 1 |