Ciprofloxacin
- Product NDC
- 50090-5671
- 11-digit product format
- 500905671
- Labeler code
- 50090
- Product ID
- 50090-5671_312e3b0f-85b8-4ed7-870f-e3f9c2282819
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076126
- Marketing category
- ANDA
- Marketing start
- 2009-10-10
- 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
- 2023-12-31
- 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 |
|---|
| 50090-5671-0 | 50090567100 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-5671-0) | 2021-09-16 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | A-S Medication Solutions | 2022-02-07 | HUMAN PRESCRIPTION DRUG LABEL | 1 |