ciprofloxacin
- Product NDC
- 68071-1893
- 11-digit product format
- 680711893
- Labeler code
- 68071
- Product ID
- 68071-1893_d606239d-e61e-0c39-e053-2995a90acaf5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ciprofloxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA076639
- Marketing category
- ANDA
- Marketing start
- 2004-09-10
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-1893-1 | 68071189301 | 20 TABLET in 1 BOTTLE (68071-1893-1) | 20 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-2 | 68071189302 | 21 TABLET in 1 BOTTLE (68071-1893-2) | 21 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-3 | 68071189303 | 30 TABLET in 1 BOTTLE (68071-1893-3) | 30 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-5 | 68071189305 | 6 TABLET in 1 BOTTLE (68071-1893-5) | 6 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-6 | 68071189306 | 60 TABLET in 1 BOTTLE (68071-1893-6) | 60 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-7 | 68071189307 | 10 TABLET in 1 BOTTLE (68071-1893-7) | 10 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-8 | 68071189308 | 28 TABLET in 1 BOTTLE (68071-1893-8) | 28 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |
| 68071-1893-9 | 68071189309 | 90 TABLET in 1 BOTTLE (68071-1893-9) | 90 tablet | 2017-03-24 | 0000-00-00 | No | No | Current |