Ciprofloxacin
- Product NDC
- 68788-7864
- 11-digit product format
- 687887864
- Labeler code
- 68788
- Product ID
- 68788-7864_8d018d3e-5f5f-49fe-879b-6fe17cf751a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2021-02-08
- 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
- 2023-12-31
- 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 |
|---|
| 68788-7864-0 | 68788786400 | 6 TABLET, FILM COATED in 1 BOTTLE (68788-7864-0) | 2021-02-08 | 0000-00-00 | No | No | Current |
| 68788-7864-1 | 68788786401 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-7864-1) | 2021-02-08 | 0000-00-00 | No | No | Current |
| 68788-7864-2 | 68788786402 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7864-2) | 2021-02-08 | 0000-00-00 | No | No | Current |
| 68788-7864-3 | 68788786403 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7864-3) | 2021-02-08 | 0000-00-00 | No | No | Current |
| 68788-7864-4 | 68788786404 | 40 TABLET, FILM COATED in 1 BOTTLE (68788-7864-4) | 2021-02-08 | 0000-00-00 | No | No | Current |
| 68788-7864-6 | 68788786406 | 60 TABLET, FILM COATED in 1 BOTTLE, DROPPER (68788-7864-6) | 2021-02-08 | 0000-00-00 | No | No | Current |
| 68788-7864-8 | 68788786408 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-7864-8) | 2021-02-08 | 0000-00-00 | No | No | Current |