Ciprofloxacin
- Product NDC
- 50090-4314
- 11-digit product format
- 500904314
- Labeler code
- 50090
- Product ID
- 50090-4314_71143abd-1c83-4c4e-bfed-8f402c467825
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076558
- 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
- 2020-12-31
- 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 |
| 5E8K9I0O4U | CIPROFLOXACIN | 85721-33-1 | Ciprofloxacin |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4314-0 | 50090431400 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-4314-0) | 2019-05-29 | 0000-00-00 | No | No | Current |
| 50090-4314-1 | 50090431401 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-4314-1) | 2019-05-29 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | A-S Medication Solutions | 2019-06-10 | HUMAN PRESCRIPTION DRUG LABEL | 1 |