Ciprofloxacin
- Product NDC
- 50090-7297
- 11-digit product format
- 500907297
- Labeler code
- 50090
- Product ID
- 50090-7297_fa78032d-254d-4305-afe9-f672e95aea29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofolxacin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA208921
- Marketing category
- ANDA
- Marketing start
- 2023-10-01
- Substance
- CIPROFLOXACIN HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Cytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7297-0 | 50090729700 | 6 TABLET in 1 BOTTLE (50090-7297-0) | 6 tablet | 2024-10-10 | No | No | Historical |
| 50090-7297-1 | 50090729701 | 14 TABLET in 1 BOTTLE (50090-7297-1) | 14 tablet | 2024-10-10 | No | No | Historical |
| 50090-7297-2 | 50090729702 | 10 TABLET in 1 BOTTLE (50090-7297-2) | 10 tablet | 2024-10-10 | No | No | Historical |
| 50090-7297-3 | 50090729703 | 3 TABLET in 1 BOTTLE (50090-7297-3) | 3 tablet | 2024-10-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin | A-S Medication Solutions | 2024-10-14 | HUMAN PRESCRIPTION DRUG LABEL | 2 |