Ciprofloxacin
- Product NDC
- 55700-608
- 11-digit product format
- 557000608
- Labeler code
- 55700
- Product ID
- 55700-608_7ed339ba-89dc-42a5-8fcd-4479c42eaf39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077859
- Marketing category
- ANDA
- Marketing start
- 2018-05-04
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4BA73M5E37 | CIPROFLOXACIN HYDROCHLORIDE | 86393-32-0 | CIPROFLOXACIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-608-06 | 55700060806 | 6 TABLET, FILM COATED in 1 BOTTLE (55700-608-06) | 2018-05-04 | 0000-00-00 | No | No | Current |
| 55700-608-10 | 55700060810 | 10 TABLET, FILM COATED in 1 BOTTLE (55700-608-10) | 2018-05-04 | 0000-00-00 | No | No | Current |
| 55700-608-14 | 55700060814 | 14 TABLET, FILM COATED in 1 BOTTLE (55700-608-14) | 2018-05-04 | 0000-00-00 | No | No | Current |
| 55700-608-20 | 55700060820 | 20 TABLET, FILM COATED in 1 BOTTLE (55700-608-20) | 2018-05-04 | 0000-00-00 | No | No | Current |