Ciprofloxacin
- Product NDC
- 68788-8088
- 11-digit product format
- 687888088
- Labeler code
- 68788
- Product ID
- 68788-8088_e6cea6af-a9a6-49af-8478-6f98f957dece
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076794
- Marketing category
- ANDA
- Marketing start
- 2021-10-05
- Marketing end
- 0000-00-00
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8088-1 | 68788808801 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8088-1) | 2021-10-05 | 0000-00-00 | No | No | Current |
| 68788-8088-2 | 68788808802 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8088-2) | 2021-10-05 | 0000-00-00 | No | No | Current |
| 68788-8088-3 | 68788808803 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8088-3) | 2021-10-05 | 0000-00-00 | No | No | Current |