Ciprofloxacin
- Product NDC
- 72189-304
- 11-digit product format
- 721890304
- Labeler code
- 72189
- Product ID
- 72189-304_2c295d71-a6a7-fce9-e063-6394a90a4492
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ciprofloxacin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DirectRx
- Application
- ANDA076558
- Marketing category
- ANDA
- Marketing start
- 2021-12-17
- 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 |
| 5E8K9I0O4U | CIPROFLOXACIN | 85721-33-1 | Ciprofloxacin |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-304-06 | 72189030406 | 6 TABLET, FILM COATED in 1 BOTTLE (72189-304-06) | 2021-12-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ciprofloxacin 250 mg | DirectRx | 2025-01-20 | HUMAN PRESCRIPTION DRUG LABEL | 2 |