Ciprofloxacin
- Product NDC
- 68788-9006
- 11-digit product format
- 687889006
- Labeler code
- 68788
- Product ID
- 68788-9006_ff470c89-9638-4e39-a5fa-aa0dfafdbe3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA075593
- Marketing category
- ANDA
- Marketing start
- 2011-06-14
- 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
- 2024-12-31
- 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 |
|---|
| 68788-9006-0 | 68788900600 | 6 TABLET, FILM COATED in 1 BOTTLE (68788-9006-0) | 2011-06-14 | 0000-00-00 | No | No | Current |
| 68788-9006-1 | 68788900601 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-9006-1) | 2011-06-14 | 0000-00-00 | No | No | Current |
| 68788-9006-2 | 68788900602 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-9006-2) | 2011-06-14 | 0000-00-00 | No | No | Current |
| 68788-9006-3 | 68788900603 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-9006-3) | 2011-06-14 | 0000-00-00 | No | No | Current |
| 68788-9006-4 | 68788900604 | 40 TABLET, FILM COATED in 1 BOTTLE (68788-9006-4) | 2011-06-14 | 0000-00-00 | No | No | Current |
| 68788-9006-6 | 68788900606 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-9006-6) | 2011-06-14 | 0000-00-00 | No | No | Current |
| 68788-9006-8 | 68788900608 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-9006-8) | 2011-06-14 | 0000-00-00 | No | No | Current |