Ciprofloxacin
- Product NDC
- 68788-7580
- 11-digit product format
- 687887580
- Labeler code
- 68788
- Product ID
- 68788-7580_0c178cee-1c69-4e5d-ac66-9684badd78f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2019-07-13
- 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 |
|---|
| 68788-7580-0 | 68788758000 | 6 TABLET, COATED in 1 BOTTLE (68788-7580-0) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7580-1 | 68788758001 | 14 TABLET, COATED in 1 BOTTLE (68788-7580-1) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7580-2 | 68788758002 | 20 TABLET, COATED in 1 BOTTLE (68788-7580-2) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7580-3 | 68788758003 | 30 TABLET, COATED in 1 BOTTLE (68788-7580-3) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7580-4 | 68788758004 | 40 TABLET, COATED in 1 BOTTLE (68788-7580-4) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7580-6 | 68788758006 | 60 TABLET, COATED in 1 BOTTLE (68788-7580-6) | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7580-8 | 68788758008 | 10 TABLET, COATED in 1 BOTTLE (68788-7580-8) | 2019-12-27 | 0000-00-00 | No | No | Current |