Ciprofloxacin
- Product NDC
- 68071-4849
- 11-digit product format
- 680714849
- Labeler code
- 68071
- Product ID
- 68071-4849_bb902533-90f8-fa5c-e053-2a95a90aa0a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Tablets
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2018-11-01
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4849-2 | 68071484902 | 20 TABLET, COATED in 1 BOTTLE (68071-4849-2) | 2019-04-15 | 0000-00-00 | No | No | Current |