Ciprofloxacin
- Product NDC
- 68071-4387
- 11-digit product format
- 680714387
- Labeler code
- 68071
- Product ID
- 68071-4387_baff690e-937c-cf8c-e053-2995a90af7cd
- 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
- 250 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4387-2 | 68071438702 | 21 TABLET, FILM COATED in 1 BOTTLE (68071-4387-2) | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4387-3 | 68071438703 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-4387-3) | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4387-4 | 68071438704 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-4387-4) | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4387-5 | 68071438705 | 20 TABLET, FILM COATED in 1 BOTTLE (68071-4387-5) | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4387-6 | 68071438706 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-4387-6) | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4387-7 | 68071438707 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-4387-7) | 2018-04-10 | 0000-00-00 | No | No | Current |
| 68071-4387-8 | 68071438708 | 28 TABLET, FILM COATED in 1 BOTTLE (68071-4387-8) | 2018-04-10 | 0000-00-00 | No | No | Current |