Ciprofloxacin
- Product NDC
- 68071-2374
- 11-digit product format
- 680712374
- Labeler code
- 68071
- Product ID
- 68071-2374_be3a7290-3bc8-2e5a-e053-2a95a90ade1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075593
- Marketing category
- ANDA
- Marketing start
- 2004-06-09
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-2374 | CIPROFLOXACIN TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.] | 2 | Legacy NDC | 20250116_be3a7290-3bc7-2e5a-e053-2a95a90ade1f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2374-2 | 68071237402 | 2 TABLET, FILM COATED in 1 BOTTLE (68071-2374-2) | 2021-03-23 | 0000-00-00 | No | No | Current |
| 68071-2374-4 | 68071237404 | 4 TABLET, FILM COATED in 1 BOTTLE (68071-2374-4) | 2021-03-23 | 0000-00-00 | No | No | Current |
| 68071-2374-6 | 68071237406 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-2374-6) | 2021-03-23 | 0000-00-00 | No | No | Current |